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Superseded
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
View Superseded by
Medical gloves for single use - Part 3: Requirements and testing for biological evaluation
Available format(s)
Hardcopy , PDF
Superseded date
01-02-2024
Superseded by
Language(s)
English, German
Published date
01-07-2015
Important note : Users cannot be edited or removed once added to your Multi user PDF.This standard is included in DIN Handbook 227/2.
| DevelopmentNote |
DRAFT AMD 1 issued in November 2016. (11/2016)
|
| DocumentType |
Standard
|
| Pages |
36
|
| PublisherName |
German Institute for Standardisation (Deutsches Institut für Normung)
|
| Status |
Superseded
|
| SupersededBy | |
| Supersedes |
| Standards | Relationship |
| NS EN 455-3 : 1999 | Identical |
| BS EN 455-3:2015 | Identical |
| I.S. EN 455-3:2015 | Identical |
| SN EN 455-3 : 2015 | Identical |
| NBN EN 455-3 : 2015 | Identical |
| UNI EN 455-3 : 2007 | Identical |
| UNE-EN 455-3:2015 | Identical |
| NF EN 455-3 : 2015 | Identical |
| EN 455-3:2015 | Identical |
| NEN EN 455-3 : 2015 | Identical |
| ONORM EN 455-3 : 2015 | Identical |
| 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 |
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