| Name |
Description |
Abstract |
Status |
Publication date |
Edition |
Number of pages |
Technical committee |
ICS |
| ISO 7459:2004 |
Glass containers — Thermal shock resistance and thermal shock endurance — Test methods |
ISO 7459:2004 specifies test methods for determining the thermal shock resistance and thermal shock endurance of glass containers.
It does not apply to the determination of properties of laboratory glassware.
|
Published |
2004-03 |
Edition : 2 |
Number of pages : 5 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 9100-1:2005 |
Glass containers — Vacuum lug finishes — Part 1: General |
ISO 9100-1:2005 specifies the types of vacuum lug finishes for glass containers for ISO 9100-2 to ISO 9100-14.
|
Published |
2005-01 |
Edition : 1 |
Number of pages : 1 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 8106:1985 |
Glass containers — Determination of capacity by gravimetric method — Test method |
The brimfull and filling capacity is calculated from the mass of the water filling the container, adjusted ba a factor for temperature and density of the water. Apparatus and procedure are described including measurement accuracy and volume correction factors.
|
Withdrawn |
1985-07 |
Edition : 1 |
Number of pages : 2 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 8106:2004 |
Glass containers — Determination of capacity by gravimetric method — Test method |
ISO 8106:2004 specifies a gravimetric method for determining the capacity of glass containers and their compliance with specification limits.
|
Published |
2004-11 |
Edition : 2 |
Number of pages : 5 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 8113:1985 |
Glass containers — Resistance to vertical load — Test method |
A method if inspection and determination of the resistance of glass containers to external force in the direction of the axis is specified. The pass tests are intended especially for containers the resistance of which is specified. The press with two horizontal flat steel pressure plates and the test method are specified.
|
Withdrawn |
1985-07 |
Edition : 1 |
Number of pages : 2 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 8113:2004 |
Glass containers — Resistance to vertical load — Test method |
ISO 8113:2004 specifies a method for determination of the resistance of glass containers to external force in the direction of the vertical axis.
|
Published |
2004-03 |
Edition : 2 |
Number of pages : 2 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 8162:1985 |
Glass containers — Tall crown finishes — Dimensions |
All needed dimensions on beverage bottles are given in a drawing, untoleranced ones being nominal. Additionaly the definitions given in ISO 7348 shall apply.
|
Withdrawn |
1985-07 |
Edition : 1 |
Number of pages : 2 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 8163:1985 |
Glass containers — Shallow crown finishes — Dimensions |
In a drawing all needed dimensions on beverage bottles are given with untoleranced as nominal ones. Additionally the definitions given in ISO 7348 shall apply.
|
Withdrawn |
1985-07 |
Edition : 1 |
Number of pages : 2 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 8164:1990 |
Glass containers — 520 ml Euro-form bottles — Dimensions |
Specifies the dimensions of Euro-form bottles, made of amber or green glass, with a tall crown cork finish, according to ISO 8162, and having a brimful capacity of 520 ml. A figure illustrates the details of shape.
|
Withdrawn |
1990-12 |
Edition : 1 |
Number of pages : 2 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 9008:1991 |
Glass bottles — Verticality — Test method |
Specifies a test method which determines not only the deviation of the whole body from the vertical, but also the combined effect of various deformations which may also be present.
|
Published |
1991-12 |
Edition : 1 |
Number of pages : 2 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 9009:1991 |
Glass containers — Height and non-parallelism of finish with reference to container base — Test methods |
Specifies test methods. Describes the principle, the apparatus, the sampling, the test procedure, the expression of results, and the contents of the test report.
|
Published |
1991-12 |
Edition : 1 |
Number of pages : 3 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 9056:1990 |
Glass containers — Series of pilferproof finish — Dimensions |
Specifies the dimensions of a series of pilferproof finishes of glass containers for non-pressurized drinks and other products. Three figures illustrate details of shapes.
|
Withdrawn |
1990-12 |
Edition : 1 |
Number of pages : 5 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 9057:1991 |
Glass containers — 28 mm tamper-evident finish for pressurized liquids — Dimensions |
Specifies the dimensions which shall be in accordance with figure 1. All untoleranced dimensions are nominal.
|
Published |
1991-12 |
Edition : 1 |
Number of pages : 2 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 9057:1991/Cor 1:2006 |
Glass containers — 28 mm tamper-evident finish for pressurized liquids — Dimensions — Technical Corrigendum 1 |
|
Published |
2006-04 |
Edition : 1 |
Number of pages : 1 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 9058:1992 |
Glass containers — Tolerances |
Specifies tolerances for glass containers of circular cross-section and nominal capacity from 50 ml to 5 000 ml.
|
Withdrawn |
1992-09 |
Edition : 1 |
Number of pages : 2 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 9058:2008 |
Glass containers — Standard tolerances for bottles |
ISO 9058:2008 specifies tolerances for glass bottles of circular cross-section and nominal capacity from 50 ml to 5 000 ml.
|
Published |
2008-03 |
Edition : 2 |
Number of pages : 2 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 9100-2:2005 |
Glass containers — Vacuum lug finishes — Part 2: 33 medium |
ISO 9100-2:2005 specifies the dimensions of a vacuum lug finish with a nominal size of 33 mm medium for wide-mouth glass containers.
|
Published |
2005-11 |
Edition : 1 |
Number of pages : 4 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 9100-2:2005/Cor 1:2009 |
Glass containers — Vacuum lug finishes — Part 2: 33 medium — Technical Corrigendum 1 |
|
Published |
2009-11 |
Edition : 1 |
Number of pages : 2 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 9100-3:2005 |
Glass containers — Vacuum lug finishes — Part 3: 38 regular |
ISO 9100-3:2005 specifies the dimensions of a vacuum lug finish with a nominal size of 38 mm regular for wide-mouth glass containers.
|
Published |
2005-11 |
Edition : 1 |
Number of pages : 4 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 9100-3:2005/Cor 1:2009 |
Glass containers — Vacuum lug finishes — Part 3: 38 regular — Technical Corrigendum 1 |
|
Published |
2009-10 |
Edition : 1 |
Number of pages : 3 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 9100-4:2005 |
Glass containers — Vacuum lug finishes — Part 4: 38 medium |
ISO 9100-4:2005 specifies the dimensions of a vacuum lug finish with a nominal size of 38 mm medium for wide-mouth glass containers.
|
Published |
2005-11 |
Edition : 1 |
Number of pages : 4 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 9100-4:2005/Cor 1:2009 |
Glass containers — Vacuum lug finishes — Part 4: 38 medium — Technical Corrigendum 1 |
|
Published |
2009-10 |
Edition : 1 |
Number of pages : 3 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 9100-5:2005 |
Glass containers — Vacuum lug finishes — Part 5: 43 and 48 regular |
ISO 9100-5:2005 specifies the dimensions of vacuum lug finishes with a nominal size of 43 mm and 48 mm regular for wide-mouth glass containers.
|
Published |
2005-01 |
Edition : 1 |
Number of pages : 5 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 9100-6:2005 |
Glass containers — Vacuum lug finishes — Part 6: 53 and 58 regular |
ISO 9100-6:2005 specifies the dimensions of vacuum lug finishes with nominal sizes of 53 mm and 58 mm regular for wide-mouth glass containers.
|
Published |
2005-01 |
Edition : 1 |
Number of pages : 5 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 9100-7:2005 |
Glass containers — Vacuum lug finishes — Part 7: 58 deep |
ISO 9100-7:2005 specifies the dimensions of vacuum lug finishes with a nominal size of 58 mm deep for wide-mouth glass containers.
|
Published |
2005-01 |
Edition : 1 |
Number of pages : 5 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 9100-8:2005 |
Glass containers — Vacuum lug finishes — Part 8: 63, 66 and 70 regular |
ISO 9100-8:2005 specifies the dimensions of vacuum lug finishes with nominal sizes of 63, 66 and 70 mm regular for wide-mouth glass containers.
|
Published |
2005-01 |
Edition : 1 |
Number of pages : 5 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 9100-9:2005 |
Glass containers — Vacuum lug finishes — Part 9: 63, 66 and 70 deep |
ISO 9100-9:2005 specifies the dimensions of vacuum lug finishes with nominal sizes of 63, 66 and 70 mm deep for wide-mouth glass containers.
|
Published |
2005-01 |
Edition : 1 |
Number of pages : 5 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 9100-10:2005 |
Glass containers — Vacuum lug finishes — Part 10: 77 regular |
ISO 9100-10:2005 specifies the dimensions of a vacuum lug finish with a nominal size of 77 mm regular for wide-mouth glass containers.
|
Published |
2005-01 |
Edition : 1 |
Number of pages : 5 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 9100-11:2005 |
Glass containers — Vacuum lug finishes — Part 11: 82 regular |
ISO 9100-11:2005 specifies the dimensions of a vacuum lug finish with a nominal size of 82 mm regular for wide-mouth glass containers.
|
Published |
2005-01 |
Edition : 1 |
Number of pages : 5 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 9100-12:2005 |
Glass containers — Vacuum lug finishes — Part 12: 89 regular |
ISO 9100-12:2005 specifies the dimensions of a vacuum lug finish with a nominal size of 89 mm regular for wide-mouth glass containers.
|
Published |
2005-01 |
Edition : 1 |
Number of pages : 5 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 9100-13:2005 |
Glass containers — Vacuum lug finishes — Part 13: 100 regular |
ISO 9100-13:2005 specifies the dimensions of a vacuum lug finish with a nominal size of 100 mm regular for wide-mouth glass containers.
|
Published |
2005-01 |
Edition : 1 |
Number of pages : 5 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 9100-14:2005 |
Glass containers — Vacuum lug finishes — Part 14: 110 regular |
ISO 9100-14:2005 specifies the dimensions of a vacuum lug finish with a nominal size of 110 mm regular for wide-mouth glass containers.
|
Published |
2005-01 |
Edition : 1 |
Number of pages : 5 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 9100-14:2005/Cor 1:2008 |
Glass containers — Vacuum lug finishes — Part 14: 110 regular — Technical Corrigendum 1 |
|
Published |
2008-10 |
Edition : 1 |
Number of pages : 2 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 9100:1992 |
Wide-mouth glass containers — Vacuum lug finishes — Dimensions |
All untoleranced dimensions specified are nominal. The glass thickness throughout the full depth of the finish shall be adequate to withstand normal handling. The finish shall be free from cracks likely to have an adverse effect on sealing performance.
|
Withdrawn |
1992-11 |
Edition : 1 |
Number of pages : 5 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 9727-1:2007 |
Cylindrical cork stoppers — Physical tests — Part 1: Determination of dimensions |
ISO 9727-1:2007 specifies a test method for determining the dimensions of cylindrical cork stoppers, namely diameter, length and, in some cases, ovalisation.
It is applicable to all types of cylindrical cork stoppers as defined in ISO 633, ready for use or semi-worked.
|
Published |
2007-05 |
Edition : 1 |
Number of pages : 3 |
Technical Committee |
55.100
Bottles. Pots. Jars
;
79.100
Cork and cork products
|
| ISO 9727-2:2007 |
Cylindrical cork stoppers — Physical tests — Part 2: Determination of mass and apparent density for agglomerated cork stoppers |
ISO 9727-2:2007 specifies a test method for measuring the mass of cylindrical cork stoppers ready for use or semi-worked, totally or partially made of agglomerated cork, and calculating the apparent density of cylindrical cork stoppers ready for use or semi-worked, totally made of agglomerated cork.
|
Published |
2007-05 |
Edition : 1 |
Number of pages : 3 |
Technical Committee |
55.100
Bottles. Pots. Jars
;
79.100
Cork and cork products
|
| ISO 9727-3:2007 |
Cylindrical cork stoppers — Physical tests — Part 3: Determination of humidity content |
ISO 9727-3:2007 specifies a test method for determining the humidity content of cylindrical cork stoppers, ready for use or semi-worked.
|
Published |
2007-05 |
Edition : 1 |
Number of pages : 3 |
Technical Committee |
55.100
Bottles. Pots. Jars
;
79.100
Cork and cork products
|
| ISO 9727-4:2007 |
Cylindrical cork stoppers — Physical tests — Part 4: Determination of dimensional recovery after compression |
ISO 9727-4:2007 specifies a test method for determining the percentage of diameter recovery of cylindrical cork stoppers, after compression.
It is applicable to all types of cylindrical cork stoppers ready for use or semi-worked, intended to be completely inserted in the bottle neck (straight cork stoppers).
|
Published |
2007-05 |
Edition : 1 |
Number of pages : 3 |
Technical Committee |
55.100
Bottles. Pots. Jars
;
79.100
Cork and cork products
|
| ISO 9727-5:2007 |
Cylindrical cork stoppers — Physical tests — Part 5: Determination of extraction force |
ISO 9727-5:2007 specifies a test method for determining the maximum force necessary to extract a cylindrical cork stopper.
It is applicable to all types of cylindrical cork stoppers ready for use, intended to be completely inserted in the bottle neck (straight cork stoppers).
|
Published |
2007-05 |
Edition : 1 |
Number of pages : 3 |
Technical Committee |
55.100
Bottles. Pots. Jars
;
79.100
Cork and cork products
|
| ISO 9727-6:2007 |
Cylindrical cork stoppers — Physical tests — Part 6: Determination of liquid tightness |
ISO 9727-6;2007 specifies a test method for determining the liquid tightness of a cylindrical cork stopper.
It is applicable to all types of cylindrical cork stoppers ready for use, intended to be completely inserted in the bottle neck (straight cork stoppers).
|
Published |
2007-05 |
Edition : 1 |
Number of pages : 3 |
Technical Committee |
55.100
Bottles. Pots. Jars
;
79.100
Cork and cork products
|
| ISO 9727-7:2007 |
Cylindrical cork stoppers — Physical tests — Part 7: Determination of dust content |
ISO 9727-7:2007 specifies a test method for determining the dust content of a cylindrical cork stopper.
It is applicable to all types of cylindrical cork stoppers ready for use, intended to be completely inserted in the bottle neck (straight cork stoppers).
|
Published |
2007-05 |
Edition : 1 |
Number of pages : 3 |
Technical Committee |
55.100
Bottles. Pots. Jars
;
79.100
Cork and cork products
|
| ISO 8536-11:2004 |
Infusion equipment for medical use — Part 11: Infusion filters for use with pressure infusion equipment |
ISO 8536-11:2004 applies to sterilized infusion filters for single use up to 200 kPa (2 bar) on fluid lines of pressure infusion equipment and infusion set as specified in ISO 8536-8. It does not include the effectiveness of filters for separation of particles or germs.
|
Withdrawn |
2004-10 |
Edition : 1 |
Number of pages : 8 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 9727-8:2022 |
Cylindrical cork stoppers — Physical tests — Part 8: Determination of capillarity |
This document specifies the test method to determine the capillarity of cylindrical cork stoppers. It consists in measuring the capillary rise by dipping in a hydro-alcoholic solution containing a dye. Two methods using the same procedure but different concentrations of hydro-alcoholic solutions are described.
It is applicable to all types of cylindrical cork stoppers, ready for use.
|
Published |
2022-04 |
Edition : 1 |
Number of pages : 4 |
Technical Committee |
55.100
Bottles. Pots. Jars
;
79.100
Cork and cork products
|
| ISO 9727:1991 |
Cylindrical stoppers of natural cork — Physical tests — Reference methods |
Specifies the reference methods for determining the following characteristics of theses stoppers: dimensions; deviations from parallelism of bases and from perpendicularity of sides and bases; apparent density; moisture content,; behaviour under compression; extraction and penetration strengths; absorption; and capillarity. Sealing behaviour will be covered later. Contains sampling, reagents, apparatur, test conditions, various tests and test report.
|
Withdrawn |
1991-02 |
Edition : 1 |
Number of pages : 9 |
Technical Committee |
55.100
Bottles. Pots. Jars
;
79.100
Cork and cork products
|
| ISO 9885:1991 |
Wide-mouth glass containers — Deviation from flatness of top sealing surface — Test methods |
Specifies two complementary methods for the determination of the deviation from flatness. Describes the principle, the apparatus, the sampling, the test procedure, the expression of results, and the contents of the test report.
|
Published |
1991-12 |
Edition : 1 |
Number of pages : 2 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 10106:2003 |
Cork stoppers — Determination of global migration |
ISO 10106:2003 specifies a test method to measure the global migration of cork stoppers.
It is applicable to all types of cork stoppers that are ready to use.
|
Withdrawn |
2003-03 |
Edition : 1 |
Number of pages : 4 |
Technical Committee |
55.100
Bottles. Pots. Jars
;
79.100
Cork and cork products
|
| ISO 10106:2018 |
Cork stoppers — Determination of global migration |
This document specifies a test method to measure the global migration of cork stoppers.
It is applicable to all types of cork stoppers that are ready to use, simulating the real conditions of use. This includes all kind of cork stoppers (completely or partially inserted in the bottle neck).
A bottle with an adequate finish is used to carry out the test.
|
Withdrawn |
2018-10 |
Edition : 2 |
Number of pages : 5 |
Technical Committee |
55.100
Bottles. Pots. Jars
;
79.100
Cork and cork products
|
| ISO 10106:2021 |
Cork stoppers — Determination of global migration |
This document specifies a test method to measure the global migration of cork stoppers.
It is applicable to all types of cork stoppers that are ready to use, simulating the real conditions of use. This includes all kind of cork stoppers (completely or partially inserted in the bottle neck).
A bottle with an adequate finish is used to carry out the test.
|
Published |
2021-06 |
Edition : 3 |
Number of pages : 5 |
Technical Committee |
55.100
Bottles. Pots. Jars
;
79.100
Cork and cork products
|
| ISO 10718:1993 |
Cork stoppers — Enumeration of colony-forming units of yeasts, moulds and bacteria capable of growth in an alcoholic medium |
The principle of the method specified consists in direct counting of the colonies by incubation in malt extract broth, using a membrane filtration procedure. Applies to cork stoppers which were submitted to sanitizing procedures and are contained in sealed packages.
|
Withdrawn |
1993-04 |
Edition : 1 |
Number of pages : 2 |
Technical Committee |
55.100
Bottles. Pots. Jars
;
79.100
Cork and cork products
;
07.100.99
Other standards related to microbiology
|
| ISO 10718:2002 |
Cork stoppers — Enumeration of colony-forming units of yeasts, moulds and bacteria capable of growth in an alcoholic medium |
ISO 10718:2002 specifies a method to enumerate the colony-forming units of yeasts, moulds and bacteria which can exist on cork stoppers and can grow in an alcoholic solution under certain conditions.
ISO 10718:2002 applies to cork stoppers which were submitted to the usual sanitizing procedures.
|
Withdrawn |
2002-08 |
Edition : 2 |
Number of pages : 6 |
Technical Committee |
55.100
Bottles. Pots. Jars
;
79.100
Cork and cork products
;
07.100.99
Other standards related to microbiology
|
| ISO 1135-4:2004 |
Transfusion equipment for medical use — Part 4: Transfusion sets for single use |
ISO 1135-4:2004 specifies requirements for single-use transfusion sets for medical use in order to ensure their compatibility with containers for blood and blood components as well as with intravenous equipment.
ISO 1135-4:2004 also specifies requirements for air-inlet devices for use with rigid containers for blood and blood components.
Secondary aims of ISO 1135-4:2004 are to provide guidance on specifications relating to the quality and performance of materials used in transfusion sets and to present designations for transfusion set components.
In some countries, the national pharmacopoeia or other national regulations are legally binding and take precedence over ISO 1135-4:2004.
|
Withdrawn |
2004-07 |
Edition : 3 |
Number of pages : 16 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 10718:2015 |
Cork stoppers — Characterization of a low-in-germs stopper, through the enumeration of colony-forming units of yeasts, moulds and bacteria, capable of both being extracted and growing in alcoholic medium |
ISO 10718:2015 specifies a method to enumerate the colony-forming units of yeasts, moulds and bacteria which can exist on cork stoppers and in an alcoholic solution, and which, under certain conditions, can be extracted during the 3 months following delivery.
ISO 10718:2015 applies to all types of ready-to-use cork stoppers, submitted to a sanitation process and packaged in properly aseptic and hermetic conditions.
ISO 10718:2015 specifies the limit values of the colony-forming units of yeasts, moulds and bacteria which can be found on cork stoppers submitted to the test procedures included in this standard.
|
Published |
2015-10 |
Edition : 3 |
Number of pages : 6 |
Technical Committee |
55.100
Bottles. Pots. Jars
;
79.100
Cork and cork products
;
07.100.99
Other standards related to microbiology
|
| ISO 12818:2013 |
Glass packaging — Standard tolerances for flaconnage |
ISO 12818:2013 specifies the tolerances for the bottles intended to be used for pharmaceutical products, cosmetic and perfumery products and chemical products. The tolerances concerned are brimful capacity, height, diameter and width, and verticality.
|
Published |
2013-06 |
Edition : 1 |
Number of pages : 9 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 12821:2013 |
Glass packaging — 26 H 180 crown finish — Dimensions |
ISO 12821:2013 specifies the dimensions of the 26-mm-tall crown finish for glass bottles containing beverages. The tall crown finish is designed to use a metal crown closure.
|
Withdrawn |
2013-09 |
Edition : 1 |
Number of pages : 6 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 12821:2019 |
Glass packaging — 26 H 180 crown finish — Dimensions |
This document specifies the dimensions of the 26 mm tall crown finish for glass bottles containing beverages. The tall crown finish is designed to use a metal crown cap (see e.g. EN 17177).
|
Published |
2019-10 |
Edition : 2 |
Number of pages : 6 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 12822:2015 |
Glass packaging — 26 H 126 crown finish — Dimensions |
ISO 12822:2015 specifies the dimensions of the 26 mm shallow crown finish for glass bottles containing beverages. The shallow crown finish is designed to use a metal crown closure (see CE.T.I.E. data sheet EC1-02 revision 1).
|
Withdrawn |
2015-08 |
Edition : 1 |
Number of pages : 5 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 12822:2020 |
Glass packaging — 26 H 126 crown finish — Dimensions |
This document specifies the dimensions of the 26 mm-shallow crown finish for glass bottles containing beverages. The shallow crown finish is designed to use a metal crown cap (see Reference [2]).
|
Published |
2020-03 |
Edition : 2 |
Number of pages : 6 |
Technical Committee |
55.100
Bottles. Pots. Jars
|
| ISO 16419:2013 |
Cork — Visual anomalies of cork stoppers for still wines |
ISO 16419:2013 applies to semi-elaborated natural cork stoppers and colmated natural cork stoppers at the definitive dimensions stage, and finished natural cork stoppers and colmated natural cork stoppers ready to use.
It describes the anomalies of cork stoppers that can be detected by visual examination by the manufacturer or the end-user.
These anomalies, according to their size, can have functional or not functional consequences being able to alter, more or less, the cork stoppers' sealing capacity.
On the basis of a common sampling example, ISO 16419:2013 proposes, for all these anomalies, some specifications for stoppers.
|
Published |
2013-01 |
Edition : 1 |
Number of pages : 6 |
Technical Committee |
55.100
Bottles. Pots. Jars
;
79.100
Cork and cork products
|
| ISO 16420:2013 |
Cork — Cork stoppers for still wines — Mechanical and physical specifications |
ISO 16420:2013 defines, for each type of ready-to-use, cylindrical cork stopper for still wines (colmated or non-colmated natural cork stoppers, agglomerate cork stoppers, 1 + 1 stoppers), a set of specifications corresponding to different tested parameters.
For all parameters, this set of specifications comprises a proposal for the number of stoppers to be tested (incremental sample); an acceptable quality level and, for certain parameters: nominal value or values; specification limits (or "tolerances").
For cork stoppers for still wines, and for certain parameters, the concept of a range is introduced, with 3 decreasing levels of requirements: upper range; standard range; entry level.
It is, therefore, up to the consumer to specify, for each batch of cork stoppers ordered, what their needs are based on these three specification levels (or ranges).
It is also up to each supplier, besides a commercial reference for each batch of cork stoppers, to define which range applies in terms of the requirements in ISO 16420:2013.
The sampling method, as well as the possible repetitions of incremental samples are defined by the sampling standard (currently being drafted) or defined jointly by the consumer and the supplier.
The stoppers tested shall comply with the requirements of ISO 9727.
|
Published |
2013-01 |
Edition : 1 |
Number of pages : 10 |
Technical Committee |
55.100
Bottles. Pots. Jars
;
79.100
Cork and cork products
|
| ISO 8871:1990/Amd 1:1995 |
Elastomeric parts for aqueous parenteral preparations — Amendment 1 |
Contains minor amendments and adds two new annexes.
|
Withdrawn |
1995-10 |
Edition : 2 |
Number of pages : 5 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 17727:2012 |
Cork — Cork stoppers for still wine — Sampling plan for the quality control of cork stoppers |
ISO 17727:2012 describes the quality control sampling plans for the receipt and shipping of ready-to-use cylindrical stoppers (flush with cork mouth finish) in semi-worked or finished cork used for still wines.
These sampling plans apply to the following parameters, for which a standardized analysis method is available. These are the parameters which are applicable to:
physical tests: dimensions, mass and apparent density for agglomerate cork stoppers, moisture content, dimensional recovery after compression, extraction force, liquid tightness and dust content (see ISO 9727);
chemical tests: analysis of oxidizing residues (see ISO 21128);
microbiological tests: enumeration of colony-forming units of yeasts, moulds and bacteria capable of growth in an alcoholic medium (see ISO 10718);
sensory analysis (see ISO 22308);
the analysis of releasable 2, 4, 6-trichloroanisole (TCA) (see ISO 20752).
|
Published |
2012-12 |
Edition : 1 |
Number of pages : 4 |
Technical Committee |
55.100
Bottles. Pots. Jars
;
79.100
Cork and cork products
|
| ISO/WD 17727 |
Cork — Cork stoppers for still wine — Sampling plan for the quality control of cork stoppers |
|
Deleted |
|
Edition : 2 |
|
Technical Committee |
55.100
Bottles. Pots. Jars
;
79.100
Cork and cork products
|
| ISO 21128:2006 |
Cork stoppers — Determination of oxidizing residues — Iodometric titration method |
ISO 21128:2006 specifies an iodometric titration method for determining the oxidizing residues released by cork stoppers ready to use.
|
Published |
2006-02 |
Edition : 1 |
Number of pages : 5 |
Technical Committee |
55.100
Bottles. Pots. Jars
;
79.100
Cork and cork products
|
| ISO/R 595:1967 |
Syringes for medical use |
|
Withdrawn |
1967-07 |
Edition : 1 |
Number of pages : 8 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO/R 596:1967 |
Withdrawal of ISO/R 596-1967 |
|
Withdrawn |
1967-12 |
Edition : 1 |
Number of pages : 4 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 1135-1:1986 |
Transfusion equipment for medical use — Part 1: Glass transfusion bottles, closures and bottle caps |
|
Withdrawn |
1986-12 |
Edition : 1 |
|
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 1135-1:1987 |
Transfusion equipment for medical use — Part 1: Glass transfusion bottles, closures and caps |
Specification of dimensions and requirements for types of transfusions bottles for medical use in order to ensure functional interchangeability of the equipment. The specifications relate also to the quality and performance of materials used in transfusion equipment. A second aim of this standard is the unified presentation of terms and designations for such equipment. This second edition of the standard constitutes a minor revision of the 1986 first one.
|
Withdrawn |
1987-10 |
Edition : 2 |
Number of pages : 9 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 1135-3:1986 |
Transfusion equipment for medical use — Part 3: Blood-taking set |
Specification of requirements for types of sterilized blood- taking sets for single use and for a single donor in order to ensure functional interchangeability of transfusion equipment. The materials and components of the sets are validated by various test methods selected by the manufacturer and, in addition, tests are provided for the release of lots of finished sets.
|
Withdrawn |
1986-11 |
Edition : 1 |
Number of pages : 8 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 1135-3:2016 |
Transfusion equipment for medical use — Part 3: Blood-taking sets for single use |
ISO 1135-3:2016 specifies requirements for types of blood-taking sets for medical use in order to ensure functional interchangeability of transfusion equipment. It is applicable to sterilized blood-taking sets intended for single use only.
ISO 1135-3:2016 also aims to provide
a) specifications relating to the quality and performance of materials used in transfusion equipment, and
b) a unified presentation of terms for such equipment.
In some countries, the national pharmacopoeia or other national regulations are legally binding and take precedence over ISO 1135-3:2016.
|
Published |
2016-11 |
Edition : 2 |
Number of pages : 12 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 1135-4:1987 |
Transfusion equipment for medical use — Part 4: Transfusion sets for single use |
|
Withdrawn |
1987-11 |
Edition : 1 |
Number of pages : 9 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 1135-4:1998 |
Transfusion equipment for medical use — Part 4: Transfusion sets for single use |
|
Withdrawn |
1998-03 |
Edition : 2 |
Number of pages : 20 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 8872:2003 |
Aluminium caps for transfusion, infusion and injection bottles — General requirements and test methods |
ISO 8872:2003 specifies general requirements and test methods for aluminium caps for injection vials, and for infusion and transfusion bottles.
|
Withdrawn |
2003-03 |
Edition : 2 |
Number of pages : 6 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 1135-4:2010 |
Transfusion equipment for medical use — Part 4: Transfusion sets for single use |
ISO 1135‑4:2010 specifies requirements for single-use transfusion sets for medical use in order to ensure their compatibility with containers for blood and blood components as well as with intravenous equipment.
Secondary aims of ISO 1135‑4:2010 are to provide guidance on specifications relating to the quality and performance of materials used in transfusion sets and to present designations for transfusion set components.
In some countries, the national pharmacopoeia or other national regulations are legally binding and take precedence over ISO 1135‑4:2010.
|
Withdrawn |
2010-04 |
Edition : 4 |
Number of pages : 15 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 1135-4:2012 |
Transfusion equipment for medical use — Part 4: Transfusion sets for single use |
ISO 1135-4:2011 specifies requirements for single-use transfusion sets for medical use in order to ensure their compatibility with containers for blood and blood components as well as with intravenous equipment.
Secondary aims of ISO 1135-4:2011 are to provide guidance on specifications relating to the quality and performance of materials used in transfusion sets and to present designations for transfusion set components.
In some countries, the national pharmacopoeia or other national regulations are legally binding and take precedence over ISO 1135-4:2011.
|
Withdrawn |
2012-03 |
Edition : 5 |
Number of pages : 15 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 1135-4:2015 |
Transfusion equipment for medical use — Part 4: Transfusion sets for single use, gravity feed |
ISO 1135-4:2015 specifies requirements for single use transfusion gravity sets for medical use in order to ensure their compatibility with containers for blood and blood components as well as with intravenous equipment.
Secondary aims of ISO 1135-4:2015 are to provide guidance on specifications relating to the quality and performance of materials used in transfusion sets, to present designations for transfusion set components, and to ensure the compatibility of sets with a range of cellular and plasma blood components.
In some countries, the national pharmacopoeia or other national regulations are legally binding and take precedence over ISO 1135-4:2015.
|
Published |
2015-12 |
Edition : 6 |
Number of pages : 16 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO/CD 1135-4 |
Transfusion equipment for medical use — Part 4: Transfusion sets for single use, gravity feed |
ISO 1135-4:2015 specifies requirements for single use transfusion gravity sets for medical use in order to ensure their compatibility with containers for blood and blood components as well as with intravenous equipment.
Secondary aims of ISO 1135-4:2015 are to provide guidance on specifications relating to the quality and performance of materials used in transfusion sets, to present designations for transfusion set components, and to ensure the compatibility of sets with a range of cellular and plasma blood components.
In some countries, the national pharmacopoeia or other national regulations are legally binding and take precedence over ISO 1135-4:2015.
|
Under development |
|
Edition : 7 |
|
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 1135-5:2015 |
Transfusion equipment for medical use — Part 5: Transfusion sets for single use with pressure infusion apparatus |
ISO 1135-5:2015 specifies requirements for single use transfusion sets for use with pressure infusion equipment capable of generating pressures up to 200 kPa (2 bar). This International Standard ensures compatibility with containers for blood and blood components as well as intravenous equipment.
Secondary aims of ISO 1135-5:2015 are to provide guidance on specifications relating to the quality and performance of materials used in transfusion sets, to present designations for transfusion set components, and to ensure the compatibility of sets with red cell and plasma blood components.
Platelet components should not be transfused under pressure using these sets.
In some countries, the national pharmacopoeia or other national regulations are legally binding and take precedence over ISO 1135-5:2015.
|
Published |
2015-12 |
Edition : 1 |
Number of pages : 20 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO/CD 1135-5 |
Transfusion equipment for medical use — Part 5: Transfusion sets for single use with pressure infusion apparatus |
ISO 1135-5:2015 specifies requirements for single use transfusion sets for use with pressure infusion equipment capable of generating pressures up to 200 kPa (2 bar). This International Standard ensures compatibility with containers for blood and blood components as well as intravenous equipment.
Secondary aims of ISO 1135-5:2015 are to provide guidance on specifications relating to the quality and performance of materials used in transfusion sets, to present designations for transfusion set components, and to ensure the compatibility of sets with red cell and plasma blood components.
Platelet components should not be transfused under pressure using these sets.
In some countries, the national pharmacopoeia or other national regulations are legally binding and take precedence over ISO 1135-5:2015.
|
Under development |
|
Edition : 2 |
|
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 1135:1977 |
Transfusion equipment for medical use |
|
Withdrawn |
1977-11 |
Edition : 1 |
Number of pages : 17 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 3825:1977 |
Glass transfusion bottles for medical use — Chemical resistance |
|
Withdrawn |
1977-09 |
Edition : 1 |
Number of pages : 2 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 3004-2:1979 |
Hermetically sealed metal containers for food and drinks — Part 2: Food cans for meat and products containing meat for human consumption |
|
Withdrawn |
1979-04 |
Edition : 1 |
Number of pages : 3 |
Technical Committee |
55.120
Cans. Tins. Tubes
|
| ISO 3826-1:2003 |
Plastics collapsible containers for human blood and blood components — Part 1: Conventional containers |
ISO 3826-1:2003 specifies requirements, including performance requirements, for plastics collapsible, non-vented, sterile containers complete with collecting tube outlet port(s), integral needle and with optional transfer tube(s), for the collection, storage, processing, transport, separation and administration of blood and blood components. The plastics containers may contain anticoagulant and/or preservative solutions, depending on the application envisaged.
ISO 3826-1:2003 is also applicable to multiple units of plastics containers, e.g. to double, triple, quadruple or multiple units.
Unless otherwise specified, all tests specified in ISO 3826-1:2003 apply to the plastics container as prepared ready for use.
ISO 3826-1:2003 is not applicable to plastics containers with an integrated filter.
|
Withdrawn |
2003-11 |
Edition : 1 |
Number of pages : 20 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 3826-1:2013 |
Plastics collapsible containers for human blood and blood components — Part 1: Conventional containers |
ISO 3826-1:2013 specifies requirements, including performance requirements, for plastics collapsible, non-vented, sterile containers complete with collecting tube outlet port(s), integral needle, and with optional transfer tube(s), for the collection, storage, processing, transport, separation, and administration of blood and blood components. The plastics containers may contain anticoagulant and/or preservative solutions, depending on the application envisaged.
ISO 3826-1:2013 is also applicable to multiple units of plastics containers, e.g. to double, triple, quadruple, or multiple units.
Unless otherwise specified, all tests specified in ISO 3826-1:2013 apply to the plastics container as prepared ready for use.
|
Withdrawn |
2013-06 |
Edition : 2 |
Number of pages : 23 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 3826-1:2019 |
Plastics collapsible containers for human blood and blood components — Part 1: Conventional containers |
This document specifies requirements, including performance requirements, for plastics collapsible, non-vented, sterile containers (known as plastics containers) complete with collecting tube outlet port(s), integral needle, and with optional transfer tube(s), for the collection, storage, processing, transport, separation, and administration of blood and blood components. The plastics containers can contain anticoagulant and/or preservative solutions, depending on the application envisaged.
This document is also applicable to multiple units of plastics containers, e.g. to double, triple, quadruple, or multiple units.
Unless otherwise specified, all tests specified in this document apply to the plastics container as prepared ready for use.
This document is not applicable to plastics containers with an integrated filter.
|
Published |
2019-09 |
Edition : 3 |
Number of pages : 23 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 3826-1:2019/Amd 1:2023 |
Plastics collapsible containers for human blood and blood components — Part 1: Conventional containers — Amendment 1 |
|
Published |
2023-03 |
Edition : 3 |
Number of pages : 1 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 3826-2:2008 |
Plastics collapsible containers for human blood and blood components — Part 2: Graphical symbols for use on labels and instruction leaflets |
ISO 3826-2:2008 addresses symbols that may be used to convey certain items of information related to medical devices dedicated to blood collection processes and storage. The information may be required on the device itself, as part of the label, or provided with the device. Many countries require that their own language be used to display textual information with medical devices. This raises problems to device manufacturers and users.
The symbols specified in ISO 3826-2:2008 do not replace current national regulatory requirements.
Manufacturers seek to take costs out of labelling by reducing or rationalizing variants. This results in a major problem of translation, design and logistics when multiple languages are included on a single label or piece of documentation. As other medical devices, blood medical devices, labelled in a number of different languages, can experience confusion and delay in locating the appropriate language. ISO 3826-2:2008 proposes solutions to these problems through the use of internationally recognized symbols with precisely defined meanings.
ISO 3826-2:2008 is primarily intended to be used by manufacturers of medical devices dedicated to the blood collection, process storage and distribution, who market identical products in countries having different language requirements for medical device labelling.
ISO 3826-2:2008 may also be of assistance to different stages of the blood supply chain, e.g.:
distributors of blood collection devices (manual or automated) or other representatives of manufacturers;
blood centres and distribution centres to simplify and secure the operating procedures.
The use of these symbols is primarily intended for the medical device rather than the therapeutic product.
|
Published |
2008-08 |
Edition : 1 |
Number of pages : 11 |
Technical Committee |
01.080.20
Graphical symbols for use on specific equipment
;
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 3826-3:2006 |
Plastics collapsible containers for human blood and blood components — Part 3: Blood bag systems with integrated features |
ISO 3826-3:2006 specifies requirements, including performance requirements, for integrated features on plastic, collapsible, non-vented, sterile containers (blood bag systems).
The integrated features refer to:
leucocyte filter;pre-donation sampling device;top and bottom bag;platelet storage bag;needle stick protection device.
In addition to ISO 3826-1:2003, which specifies the requirements of conventional containers, ISO 3826-3:2006 specifies additional requirements for blood bag systems using multiple units.
Unless otherwise specified, all tests specified in ISO 3826-3:2006 apply to the plastic container as prepared ready for use.
|
Published |
2006-09 |
Edition : 1 |
Number of pages : 9 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 8362-4:1989 |
Injection containers for injectables and accessories — Part 4: Injection vials made of moulded glass |
Specifies the dimensions, capacity, type of glass material, form and requirements of glas vails for medical use. It includes procedures for the measurement of the chemical resistivity of the inner surface of vails and, thus, enables a classification in accordance with their propper category of application.
|
Withdrawn |
1989-11 |
Edition : 1 |
Number of pages : 6 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 3826-4:2015 |
Plastics collapsible containers for human blood and blood components — Part 4: Aphaeresis blood bag systems with integrated features |
ISO 3826-4:2015 specifies requirements including performance requirements for aphaeresis blood bag systems with integrated features. Aphaeresis blood bag systems need not contain all of the integrated features identified in this part of ISO 3826.
The integrated features refer to: needle stick protection device, leucocyte filter, sterile barrier filter, pre-collection sampling device, red blood cell storage bag, plasma storage bag, platelet storage bag, polymorphonucleic (e.g. stem) cell storage bag, post-collection sampling devices, and connections for storage solutions, anticoagulant, and replacement fluid.
ISO 3826-4:2015 specifies additional requirements for blood bag systems used to collect varying quantities of blood components or cells by apheresis. It can be used on automated or semi-automated blood collection systems.
|
Published |
2015-08 |
Edition : 1 |
Number of pages : 31 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 3826:1993 |
Plastics collapsible containers for human blood and blood components |
Specifies requirements, including performance requirements (dimensions, design, conditions of manufacture, sterilization, transparency, coloration, thermal stability, vapour transmission, resistance to distortion, resistance to leakage, chemical requirements, biological requirements, packaging, marking and labelling) for di-(2-ethylhexyl)phthalate plasticized polyvinyl chloride for complete plastics collapsible, non-vented, sterile containers.
|
Withdrawn |
1993-03 |
Edition : 1 |
Number of pages : 16 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 4822:1981 |
Single use blood specimen containers up to 25 ml capacity |
|
Withdrawn |
1981-04 |
Edition : 1 |
Number of pages : 4 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 6009:1981 |
Hypodermic needles for single use — Colour coding for identification |
|
Withdrawn |
1981-04 |
Edition : 1 |
Number of pages : 3 |
Technical Committee |
01.070
Colour coding
;
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 6009:1988 |
Hypodermic needles for single use — Colour coding for identification |
|
Withdrawn |
1988-08 |
Edition : 2 |
Number of pages : 3 |
Technical Committee |
01.070
Colour coding
;
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 6710:1995 |
Single-use containers for venous blood specimen collection |
Specifies requirements and test methods for evacuated and non-evacuated single-use venous blood specimen containers. Does not apply for blood collection needles.
|
Withdrawn |
1995-08 |
Edition : 1 |
Number of pages : 12 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 6710:2017 |
Single-use containers for human venous blood specimen collection |
ISO 6710:2017 specifies requirements and test methods for evacuated and non-evacuated single-use venous blood specimen containers.
It does not specify requirements for blood collection needles, needle holders, blood culture receptacles or "arterial" blood gas collection devices that can be used for venous blood.
|
Published |
2017-07 |
Edition : 2 |
Number of pages : 15 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 7864:1984 |
Sterile hypodermic needles for single use |
|
Withdrawn |
1984-08 |
Edition : 1 |
Number of pages : 7 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 7864:1988 |
Sterile hypodermic needles for single use |
|
Withdrawn |
1988-08 |
Edition : 2 |
Number of pages : 7 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 7885:1996 |
Sterile, single-use dental injection needles |
|
Withdrawn |
1996-08 |
Edition : 1 |
Number of pages : 5 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
;
11.060.20
Dental equipment
|
| ISO 7886:1984 |
Sterile hypodermic syringes for single use |
|
Withdrawn |
1984-09 |
Edition : 1 |
Number of pages : 13 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 8362-1:1989 |
Injection containers for injectables and accessories — Part 1: Injection vials made of glass tubing |
Specification of form, dimensions, material, designations, performance and capacity of injection vails made of colourless or amber-coloured glass tubing which are used for packaging, storage or transport of products intended for injections.
|
Withdrawn |
1989-10 |
Edition : 1 |
Number of pages : 4 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|