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ONORM EN 455-3 : 2015

Superseded

Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

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superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

MEDICAL GLOVES FOR SINGLE USE - PART 3: REQUIREMENTS AND TESTING FOR BIOLOGICAL EVALUATION

Superseded date

01-20-2024

Published date

01-12-2013

Dieser Teil der EN 455 legt Anforderungen für die Bewertung der biologischen Sicherheit von medizinischen Einmalhandschuhen fest. Er enthält Anforderungen für die Kennzeichnung und die Angaben von Informationen über die angewendeten Prüfmethoden. Diese ÖNORM legt Prüfverfahren für die Biokompatibilität und Anforderungen an die Kennzeichnung der Biokompatibilität medizinischer Handschuhe zum einmaligen Gebrauch fest. Diese Norm enthält ebenfalls einen Überblick über immunologische Verfahren für die Bestimmung löslicher Proteine und Allergene.

Committee
TC 179
DocumentType
Standard
PublisherName
Osterreichisches Normungsinstitut/Austrian Standards
Status
Superseded
SupersededBy

Standards Relationship
I.S. EN 455-3:2015 Identical
SN EN 455-3 : 2015 Identical
UNI EN 455-3 : 2007 Identical
UNE-EN 455-3:2015 Identical
NS EN 455-3 : 1999 Identical
BS EN 455-3:2015 Identical
NBN EN 455-3 : 2015 Identical
NF EN 455-3 : 2015 Identical
EN 455-3:2015 Identical
NEN EN 455-3 : 2015 Identical
DIN EN 455-3:2015-07 Identical

ONORM EN 13718-2 : 2015 MEDICAL VEHICLES AND THEIR EQUIPMENT - AIR AMBULANCES - PART 2: OPERATIONAL AND TECHNICAL REQUIREMENTS FOR AIR AMBULANCES

ONORM EN 1041 : 2013 INFORMATION SUPPLIED BY THE MANUFACTURER WITH MEDICAL DEVICES
ISO 10993-10:2010 Biological evaluation of medical devices Part 10: Tests for irritation and skin sensitization
ONORM EN ISO 10993-10 : 2014 BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 10: TESTS FOR IRRITATION AND SKIN SENSITIZATION (ISO 10993-10:2010)
ISO 10993-1:2009 Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process
ONORM EN ISO 10993-1 : 2011 BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 1: EVALUATION AND TESTING WITHIN A RISK MANAGEMENT PROCESS
ISO 14971:2007 Medical devices Application of risk management to medical devices
ISO 21171:2006 Medical gloves — Determination of removable surface powder
ISO 15223-1:2016 Medical devices Symbols to be used with medical device labels, labelling and information to be supplied Part 1: General requirements

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