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All the standards published after 01 Oct 2025 are available in new portal. Please click here to view the portal
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Basic Details/ मूल ब्यौरा
Comment
IS Number/
आईएस संख्या
:
IS/ISO 13022:2012
ISO 13022 : 2012
IS Title/
आईएस शीर्षक
:
Medical products containing viable human cells - Application of risk management and requirements for processing practices
Superseding IS/
सुपरसीडिंग आईएस
:
None
Degree of Equivalence/
समतुल्यता स्तर
:
Identical under single numbering
Number of Revisions/
पुनरीक्षणों की संख्या
:
New Standard
Number of Amendments/
संशोधनों की संख्या
:
No amendment issued
Aspect/
पक्ष
:
Methods of tests
Language/
भाषा
:
English
Reaffirmation Year/
पुनर्पुष्टि वर्ष
:
Technical Department/
तकनीकी विभाग
:
MHD (Medical Equipment and Hospital Planning Department)
Technical Committee/
तकनीकी समिति
:
MHD 19 (In-vitro Diagnostic Medical Devices and Biological Evaluation of Medical Devices Sectional Committee)
Member Secretary/
सदस्य सचिव
:
Mr. KATIPALLY KARTHIK REDDY (SCIENTIST-B)
Other Details
Indian Standard
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Amendment : 0
Gazette Document : 1
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License : 0
Product Manual & SIT : 0
Laboratory : 0
Classification Details
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Cross Reference Details
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Composition
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Corrigendum : 0
Cross Reference Details
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Indian Standards Referred In IS IS/ISO 13022:2012
ISO 13022 : 2012
:
1
IS/ISO 13485:2016
Medical Devices — Quality Management Systems — Requirements for Regulatory Purposes ( First Revision )
MHD 14
International Standards Referred In IS/ISO 13022:2012
ISO 13022 : 2012
1
ISO 14971 : 0 : 0 0
2
ISO 22442 : 1 : 0 0
3
ASTM 0 : 0 : 0 0
4
BSI 0 : 0 : 0 0
IS/ISO 13022:2012
ISO 13022 : 2012
is Referred in following Indian Standards :
Standard contains no Cross Referenced Indian Standard.
Classification Details
Group
:
Medical and Hospital Equipments
Sub Group
:
Clinical, pathological, anaesthetic and respiratory equipments and systems
Sub Sub Group
:
Biological tests
Aspect
:
Methods of tests
Certification
:
