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  3. AAMI/ISO 14937:2009/(R)2013 PDF

AAMI/ISO 14937:2009/(R)2013 PDF

AAMI/ISO 14937:2009/(R)2013 PDF

Name:
AAMI/ISO 14937:2009/(R)2013 PDF

Published Date:
10/14/2009

Status:
Active

Description:

Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices

Publisher:
Association for the Advancement of Medical Instrumentation/International Org. for Standardization

Document status:
Active
Format:
Electronic (PDF)
Delivery time:
10 minutes
Delivery time (for Russian version):
200 business days
SKU:
Choose Document Language:
$71.1
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Specifies general requirements for the characterization of a sterilizing agent and for the development, validation and routine monitoring and control of a sterilization process for medical devices. Applies to sterilization processes in which microorganisms are inactivated by physical and/or chemical means. Intended to be applied by process developers, manufacturers of sterilization equipment, manufacturers of products to be sterilized and organizations responsible for sterilizing medical devices.
ANSI : ANSI Approved
File Size : 1 file , 320 KB
ISBN(s) : 1570203695
Note : This product is unavailable in Ukraine, Russia, Belarus
Number of Pages : 53
Part of : AAMI STBK10-3
Published : 10/14/2009

History

AAMI/ISO 14937:2009/(R)2013
AAMI/ISO 14937:2009/(R)2013
Published Date: 10/14/2009
Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices
$71.1
AAMI/ISO 14937:2000
AAMI/ISO 14937:2000
Published Date: 03/13/2000
Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices
$29.7
AAMI/ISO 14937
AAMI/ISO 14937
Published Date: 03/13/2000
Sterilization of health care products- General requirements for characterization of a sterlizing agent and the development, validation, and routine control of a sterilization process for medical devices
$33

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