DIN EN 455-3:2015-07

Superseded

Superseded A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.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

Available format(s): Hardcopy, PDF

Superseded date: 01-02-2024

Language(s): English, German

Published date: 01-07-2015

Abstract - (Show below) - (Hide below)

This standard is included in DIN Handbook 227/2.

Development Note	DRAFT AMD 1 issued in November 2016. (11/2016)
Document Type	Standard
ISBN
Pages
Published
Publisher	German Institute for Standardisation (Deutsches Institut für Normung)
Status	Superseded
Superseded By	DIN EN 455-3:2024-02
Supersedes	DIN EN 455-3:2007-03

DGUV GRUNDSATZ 304-002 : 2016
BWB TL 6515-0130 : 3ED 2007
DIN 13167:2014-01	FIRST AID MATERIAL TO BE CARRIED ON MOTORCYCLES
DGUV GRUNDSATZ 304-001 : 2016	ERMAECHTIGUNG VON STELLEN FUER DIE AUS- UND FORTBILDUNG IN DER ERSTEN HILFE
VDI 2083 Blatt 9.2:2017-01	Cleanroom technology - Consumables in the cleanroom
DIN HDBK 227/2 : 5ED 2016	MEDIZINISCHE EINMALPRODUKTE - BAND 2: HAEMODIALYSE, DRAINAGEN UND KATHETER, HANDSCHUHE, KONDOME SOWIE INKONTINENZ- UND OSTOMIEHILFEN
DIN HDBK 257 : 4ED 2013

EN ISO 10993-5:2009	Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009)
EN ISO 10993-10:2013	Biological evaluation of medical devices - Part 10: Tests for irritation and skin sensitization (ISO 10993-10:2010)
EN 1041:2008+A1:2013	Information supplied by the manufacturer of medical devices
ISO 10993-10:2010	Biological evaluation of medical devices Part 10: Tests for irritation and skin sensitization
ISO 10993-1:2009	Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process
EN ISO 21171:2006	Medical gloves - Determination of removable surface powder (ISO 21171:2006)
EN ISO 14971:2012	Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01)
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
EN ISO 10993-1:2009/AC:2010	BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 1: EVALUATION AND TESTING WITHIN A RISK MANAGEMENT PROCESS (ISO 10993-1:2009/COR 1:2010)

Product Format

Quantity

Buy now

Add to cart

Create account

This standard is included in DIN Handbook 227/2.

Development Note	DRAFT AMD 1 issued in November 2016. (11/2016)
Document Type	Standard
ISBN
Pages
Published
Publisher	German Institute for Standardisation (Deutsches Institut für Normung)
Status	Superseded
Superseded By	DIN EN 455-3:2024-02
Supersedes	DIN EN 455-3:2007-03

DGUV GRUNDSATZ 304-002 : 2016
BWB TL 6515-0130 : 3ED 2007
DIN 13167:2014-01	FIRST AID MATERIAL TO BE CARRIED ON MOTORCYCLES
DGUV GRUNDSATZ 304-001 : 2016	ERMAECHTIGUNG VON STELLEN FUER DIE AUS- UND FORTBILDUNG IN DER ERSTEN HILFE
VDI 2083 Blatt 9.2:2017-01	Cleanroom technology - Consumables in the cleanroom
DIN HDBK 227/2 : 5ED 2016	MEDIZINISCHE EINMALPRODUKTE - BAND 2: HAEMODIALYSE, DRAINAGEN UND KATHETER, HANDSCHUHE, KONDOME SOWIE INKONTINENZ- UND OSTOMIEHILFEN
DIN HDBK 257 : 4ED 2013

EN ISO 10993-5:2009	Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009)
EN ISO 10993-10:2013	Biological evaluation of medical devices - Part 10: Tests for irritation and skin sensitization (ISO 10993-10:2010)
EN 1041:2008+A1:2013	Information supplied by the manufacturer of medical devices
ISO 10993-10:2010	Biological evaluation of medical devices Part 10: Tests for irritation and skin sensitization
ISO 10993-1:2009	Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process
EN ISO 21171:2006	Medical gloves - Determination of removable surface powder (ISO 21171:2006)
EN ISO 14971:2012	Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01)
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
EN ISO 10993-1:2009/AC:2010	BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 1: EVALUATION AND TESTING WITHIN A RISK MANAGEMENT PROCESS (ISO 10993-1:2009/COR 1:2010)