Comment Closes On
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Development Note
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Supersedes DIN EN 866-6 and DIN EN 866-6 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
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Superseded |
Supersedes
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DIN EN ISO 20857 E : 2013
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STERILIZATION OF HEALTH CARE PRODUCTS - DRY HEAT - REQUIREMENTS FOR THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES (ISO 20857:2010) |
VDI 6300 Blatt 1:2016-05
|
Genetic engineering operations in genetic engineering facilities - Guidance on safe operation of genetic engineering facilities |
DIN EN ISO 20857:2013-08
|
Sterilization of health care products - Dry heat - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 20857:2010) |
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 20857:2013-08
|
Sterilization of health care products - Dry heat - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 20857:2010) |
DIN EN ISO 14161:2010-03
|
STERILIZATION OF HEALTH CARE PRODUCTS - BIOLOGICAL INDICATORS - GUIDANCE FOR THE SELECTION, USE AND INTERPRETATION OF RESULTS |
ISO 18472:2006
|
Sterilization of health care products Biological and chemical indicators Test equipment |
ISO 20857:2010
|
Sterilization of health care products Dry heat Requirements for the development, validation and routine control of a sterilization process for medical devices |
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 |
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