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SRPS EN ISO 3826-3:2011

Plastics collapsible containers for human blood and blood components - Part 3: Blood bag systems with integrated features (ISO 3826-3:2006)

Jun 28, 2011

General information

60.60     Jun 28, 2011

ISS

Z076

European Norm

11.040.20  

English  

From plan 2011

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Scope

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.

Related directives

NOTE: If the word "harmonized" (marked in green) is not found in the field with the name of the directive, it means that the European standard is not cited in the OJEU.

93/42/EEC

Medical devices

Harmonized

Life cycle

NOW

PUBLISHED
SRPS EN ISO 3826-3:2011
60.60 Standard published
Jun 28, 2011

REVISED BY

PROJECT
naSRPS EN ISO 3826-3:2024

Related project

Adopted from EN ISO 3826-3:2007

Adopted from ISO 3826-3:2006 IDENTICAL