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Norm
ÖNORM EN ISO 3826-1
Issue date: 2013 09 01
Plastics collapsible containers for human blood and blood components - Part 1: Conventional containers (ISO 3826-1:2013)
This part of ISO 3826 specifies requirements, including performance requirements, for plastics
collapsible, non-vented, sterile containers complete with collecting tube ...
Read more
Withdrawn
: 2020 02 01
Publisher:
Austrian Standards International
Format:
Digital | 31 Pages
Language:
German
| English
Currently valid:
Optionally co-design standards:
ICS
This part of ISO 3826 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.
This part of ISO 3826 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 part of ISO 3826 apply to the plastics container as
prepared ready for use.
This part of ISO 3826 is not applicable to plastics containers with an integrated filter.
ÖNORM EN ISO 3826-1
2020 02 01
Plastics collapsible containers for human blood and blood components - Part 1: Conventional containe...
Norm
ÖNORM EN ISO 3826-1
2013 09 01
Plastics collapsible containers for human blood and blood components - Part 1: Conventional containe...
Norm
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ÖNORM EN ISO 3826-1
2004 03 01
Plastics collapsible containers for human blood and blood components - Part 1: Conventional containe...
Norm
Norm
ISO 10993-1:2009
Issue date :
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ISO 10993-4:2002
Issue date :
2002 10 22
Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood
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ISO 10993-5:2009
Issue date :
2009 05 20
Biological evaluation of medical devices — Part 5: Tests for in vitro cytotoxicity
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ISO 10993-10:2010
Issue date :
2010 07 27
Biological evaluation of medical devices — Part 10: Tests for irritation and skin sensitization
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ISO 10993-11:2006
Issue date :
2006 08 15
Biological evaluation of medical devices — Part 11: Tests for systemic toxicity
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ISO 10993-12:2012
Issue date :
2012 06 29
Biological evaluation of medical devices — Part 12: Sample preparation and reference materials
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ISO 1135-4:2012
Issue date :
2012 02 24
Transfusion equipment for medical use — Part 4: Transfusion sets for single use
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ISO 3696:1987
Issue date :
1987 04 09
Water for analytical laboratory use — Specification and test methods
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ISO 10993-11:2017
Issue date :
2017 09 14
Biological evaluation of medical devices — Part 11: Tests for systemic toxicity
Norm
ÖNORM EN ISO 3826-1
Issue date :
2020 02 01
Plastics collapsible containers for human blood and blood components - Part 1: Conventional containers (ISO 3826-1:2019)
Norm
ISO 3826-1:2013
Issue date :
2013 05 16
Plastics collapsible containers for human blood and blood components — Part 1: Conventional containers