ISO 3826-4 Plastics collapsible containers for human blood and blood components - Part 4: Aphaeresis blood bag systems with integrated features - First Edition
Данный раздел/документ содержится в продуктах:
- Техэксперт: Машиностроительный комплекс
- Картотека зарубежных и международных стандартов
- ISO 3826-4 Plastics collapsible containers for human blood and blood components - Part 4: Aphaeresis blood bag systems with integrated features - First Edition
- 11
- ISO 3826-4 Plastics collapsible containers for human blood and blood components - Part 4: Aphaeresis blood bag systems with integrated features - First Edition
- 11.040
- ISO 3826-4 Plastics collapsible containers for human blood and blood components - Part 4: Aphaeresis blood bag systems with integrated features - First Edition
- 11.040.20
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- ASTM D4169 Standard Practice for Performance Testing of Shipping Containers and Systems
- ASTM D5414 Standard Test Method for Evaluation of Horizontal Impact Performance of Load Unitizing Stretch Wrap Films
- ASTM D4649 Standard Guide for Selection and Use of Stretch Wrap Films
- ASTM D5458 Standard Test Method for Peel Cling of Stretch Wrap Film
- ASTM D5458 Standard Test Method for Peel Cling of Stretch Wrap Film
- ASTM D4649 Standard Guide for Selection and Use of Stretch Wrap Films
- ASTM D5414 Standard Test Method for Evaluation of Horizontal Impact Performance of Load Unitizing Stretch Wrap Films
- ASTM D4169 Standard Practice for Performance Testing of Shipping Containers and Systems
- UL 61010-2-101 BULLETIN UL Standard for Safety Electrical Equipment for Measurement, Control, and Laboratory Use – Part 2-101: Particular Requirements for In Vitro Diagnostic (IVD) Medical Equipment - COMMENTS DUE: JULY 27, 2015
- ISO 15223-1 Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements - Second Edition
- UL 61010-2-101 BULLETIN UL Standard for Safety Electrical Equipment for Measurement, Control, and Laboratory Use – Part 2-101: Particular Requirements for In Vitro Diagnostic (IVD) Medical Equipment - COMMENTS DUE: JULY 27, 2015
- ASTM D4169 Standard Practice for Performance Testing of Shipping Containers and Systems
- ASTM D5414 Standard Test Method for Evaluation of Horizontal Impact Performance of Load Unitizing Stretch Wrap Films
- ASTM D4649 Standard Guide for Selection and Use of Stretch Wrap Films
- ASTM D4649 Standard Guide for Selection and Use of Stretch Wrap Films
- ASTM D5414 Standard Test Method for Evaluation of Horizontal Impact Performance of Load Unitizing Stretch Wrap Films
- ASTM D4169 Standard Practice for Performance Testing of Shipping Containers and Systems
- UL 61010-2-101 BULLETIN UL Standard for Safety Electrical Equipment for Measurement, Control, and Laboratory Use – Part 2-101: Particular Requirements for In Vitro Diagnostic (IVD) Medical Equipment - COMMENTS DUE: JULY 27, 2015
- ISO 15223-1 Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements - Second Edition
- UL 61010-2-101 BULLETIN UL Standard for Safety Electrical Equipment for Measurement, Control, and Laboratory Use – Part 2-101: Particular Requirements for In Vitro Diagnostic (IVD) Medical Equipment - COMMENTS DUE: JULY 27, 2015
- ASTM D4169 Standard Practice for Performance Testing of Shipping Containers and Systems
- ASTM D5414 Standard Test Method for Evaluation of Horizontal Impact Performance of Load Unitizing Stretch Wrap Films
- ASTM D5414 Standard Test Method for Evaluation of Horizontal Impact Performance of Load Unitizing Stretch Wrap Films
- ASTM D4169 Standard Practice for Performance Testing of Shipping Containers and Systems
- UL 61010-2-101 BULLETIN UL Standard for Safety Electrical Equipment for Measurement, Control, and Laboratory Use – Part 2-101: Particular Requirements for In Vitro Diagnostic (IVD) Medical Equipment - COMMENTS DUE: JULY 27, 2015
- ISO 15223-1 Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements - Second Edition
- UL 61010-2-101 BULLETIN UL Standard for Safety Electrical Equipment for Measurement, Control, and Laboratory Use – Part 2-101: Particular Requirements for In Vitro Diagnostic (IVD) Medical Equipment - COMMENTS DUE: JULY 27, 2015
- ASTM D4169 Standard Practice for Performance Testing of Shipping Containers and Systems
- ASTM D4169 Standard Practice for Performance Testing of Shipping Containers and Systems
- UL 61010-2-101 BULLETIN UL Standard for Safety Electrical Equipment for Measurement, Control, and Laboratory Use – Part 2-101: Particular Requirements for In Vitro Diagnostic (IVD) Medical Equipment - COMMENTS DUE: JULY 27, 2015
- ISO 15223-1 Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements - Second Edition
- UL 61010-2-101 BULLETIN UL Standard for Safety Electrical Equipment for Measurement, Control, and Laboratory Use – Part 2-101: Particular Requirements for In Vitro Diagnostic (IVD) Medical Equipment - COMMENTS DUE: JULY 27, 2015
- UL 61010-2-101 BULLETIN UL Standard for Safety Electrical Equipment for Measurement, Control, and Laboratory Use – Part 2-101: Particular Requirements for In Vitro Diagnostic (IVD) Medical Equipment - COMMENTS DUE: JULY 27, 2015
- ISO 15223-1 Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements - Second Edition
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- Картотека зарубежных и международных стандартов
International Organization for Standardization
Plastics collapsible containers for human blood and blood components - Part 4: Aphaeresis blood bag systems with integrated features - First Edition
N 3826-4
Annotation
This part of ISO 3826 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.
This part of ISO 3826 specifies additional requirements for blood bag systems used to collect varying quantities of blood components or cells by apheresis. This part of ISO 3826 can be used on automated or semi-automated blood collection systems.
In some countries, the national pharmacopoeia or other national regulations are legally binding and take precedence over this part of ISO 3826.



