ONORM EN ISO 3826-1 : 2013
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
View Superseded by
PLASTICS COLLAPSIBLE CONTAINERS FOR HUMAN BLOOD AND BLOOD COMPONENTS - PART 1: CONVENTIONAL CONTAINERS (ISO 3826-1:2013)
01-02-2020
12-01-2013
Diese ÖNORM legt allgemeine und Funktionsanforderungen fest an unbelüftete weiche und sterile Behälter aus Kunststoff für die Spende, Lagerung, Verarbeitung, Transport, Trennung und Bereitstellung von Blut und Blutbestandteilen. Die Kunststoffbehälter können Antigerinnungsmittel und/oder andere Konservierungsstoffe enthalten. Mit eingeschlossen sind die Schläuche, Ein- und Ausgänge und eventuelle Zusatzbehälter.
DocumentType |
Standard
|
PublisherName |
Osterreichisches Normungsinstitut/Austrian Standards
|
Status |
Withdrawn
|
SupersededBy |
Standards | Relationship |
I.S. EN ISO 3826-1:2013 | Identical |
UNI EN ISO 3826-1 : 2013 | Identical |
NS EN ISO 3826-1 : 2013 | Identical |
BS EN ISO 3826-1:2013 | Identical |
SN EN ISO 3826-1 : 2013 | Identical |
NBN EN ISO 3826-1 : 2013 | Identical |
UNE-EN ISO 3826-1:2013 | Identical |
EN ISO 3826-1:2013 | Identical |
NEN EN ISO 3826-1 : 2013 | Identical |
ISO 3826-1:2013 | Identical |
NF EN ISO 3826-1 : 2013 | Identical |
DIN EN ISO 3826-1:2013-09 | Identical |
ISO 10993-4:2017 | Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood |
ISO 10993-10:2010 | Biological evaluation of medical devices Part 10: Tests for irritation and skin sensitization |
ISO 10993-11:2017 | Biological evaluation of medical devices — Part 11: Tests for systemic toxicity |
ISO 10993-12:2012 | Biological evaluation of medical devices Part 12: Sample preparation and reference materials |
ISO 10993-1:2009 | Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process |
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