Comment Closes On
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Committee
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TC 198 |
Development Note
|
Supersedes DIN EN 866-3, DIN EN 866-3 E, DIN EN 866-7 and DIN EN 866-7 E. (10/2006) |
Document Type
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Draft |
ISBN
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|
Pages
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|
Published
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Publisher
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German Institute for Standardisation (Deutsches Institut für Normung)
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Status
|
Superseded |
Superseded By
|
|
Supersedes
|
|
DIN EN ISO 15882:2008-12
|
STERILIZATION OF HEALTH CARE PRODUCTS - CHEMICAL INDICATORS - GUIDANCE FOR SELECTION, USE AND INTERPRETATION OF RESULTS |
VDI 6300 Blatt 1:2016-05
|
Genetic engineering operations in genetic engineering facilities - Guidance on safe operation of genetic engineering facilities |
DIN EN ISO 14161:2010-03
|
STERILIZATION OF HEALTH CARE PRODUCTS - BIOLOGICAL INDICATORS - GUIDANCE FOR THE SELECTION, USE AND INTERPRETATION OF RESULTS |
DIN EN ISO 14534:2015-08
|
Ophthalmic optics - Contact lenses and contact lens care products - Fundamental requirements (ISO 14534:2011) |
DIN HDBK 265 : 2ED 2012
|
STERILISATION VON MEDIZINPRODUKTEN - INDIKATOREN UND VERPACKUNGEN FUER IN DER ENDVERPACKUNG ZU STERILISIERENDE MEDIZINPRODUKTE |
DIN EN ISO 14161:2010-03
|
STERILIZATION OF HEALTH CARE PRODUCTS - BIOLOGICAL INDICATORS - GUIDANCE FOR THE SELECTION, USE AND INTERPRETATION OF RESULTS |
DIN EN ISO 17665-1:2006-11
|
Sterilization of health care products - Moist heat - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 17665-1:2006) |
ISO 18472:2006
|
Sterilization of health care products Biological and chemical indicators Test equipment |
DIN EN ISO 11138-1:2015-10 (Draft)
|
STERILIZATION OF HEALTH CARE PRODUCTS - BIOLOGICAL INDICATORS - PART 1: GENERAL REQUIREMENTS (ISO 11138-1:2017) |
DIN EN ISO 18472:2006-10
|
STERILIZATION OF HEALTH CARE PRODUCTS - BIOLOGICAL AND CHEMICAL INDICATORS - TEST EQUIPMENT |
ISO 11138-1:2017
|
Sterilization of health care products — Biological indicators — Part 1: General requirements |
ISO 14161:2009
|
Sterilization of health care products Biological indicators Guidance for the selection, use and interpretation of results |
ISO 17665-1:2006
|
Sterilization of health care products — Moist heat — Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices |
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