ISO 11140-1:2005 PDF

ISO 11140-1:2005 PDF

Name:
ISO 11140-1:2005 PDF

Published Date:
07/15/2005

Status:
Active

Description:

Sterilization of health care products - Chemical indicators - Part 1: General requirements

Publisher:
International Organization for Standardization

Document status:
Active

Format:
Electronic (PDF)

Delivery time:
10 minutes

Delivery time (for Russian version):
200 business days

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$46.8
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This part of ISO 11140 specifies general requirements and test methods for indicators that show exposure to sterilization processes by means of physical and/or chemical change of substances, and which are used to monitor the attainment of one or more of the variables required for a sterilization process. They are not dependent for their action on the presence or absence of a living organism.

The requirements and test methods of this part of ISO 11140 apply to all indicators specified in subsequent parts of ISO 11140, unless the requirement is modified or added to by a subsequent part, in which case the requirement of that particular part will apply.

Relevant test equipment is described in ISO 18472.


File Size : 1 file , 340 KB
Note : This product is unavailable in Ukraine, Russia, Belarus
Number of Pages : 27
Published : 07/15/2005
Same As : ISO 11140-1:2005

History

ISO 11140-1:2014
Published Date: 11/01/2014
Sterilization of health care products - Chemical indicators - Part 1: General requirements
$58.2
ISO 11140-1:2005
Published Date: 07/15/2005
Sterilization of health care products - Chemical indicators - Part 1: General requirements
$46.8

Related products

ISO 13683:1997
Published Date: 05/15/1997
Sterilization of health care products -- Requirements for validation and routine control of moist heat sterilization in health care facilities
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ISO 11140-2:1998
Published Date: 12/01/1998
Sterilization of health care products -- Chemical indicators -- Part 2: Test equipment and methods
$14.4
ISO 17665:2024
Published Date: 03/01/2024
Sterilization of health care products - Moist heat - Requirements for the development, validation and routine control of a sterilization process for medical devices
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