| IS Number : | IS/ISO 13022 : 2012 ISO 13022 : 2012 |
|---|---|
| IS Title [Eng-Hn] : | Medical products containing viable human cells - Application of risk management and requirements for processing practices |
| No of Revision : | 0 |
| No of Amendments : | 0 |
| Technical Department : | Medical Equipment and Hospital Planning Department |
| Technical Committee : | MHD 19 ( In-vitro Diagnostic Medical Devices and Biological Evaluation of Medical Devices ) |
| Language : | English |
| Group : | Medical and Hospital Equipments |
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| Sub Group: | Clinical, pathological, anaesthetic and respiratory equipments and systems |
| Sub Sub Group : | Biological tests |
| Aspects: | Methods of tests |
| Certification: | |
| Ministry : | Ministry of Health and Family Welfare |
| Short Commom Man's Title: | |
| Itchs: | N/A |
| Degree of Equivalence: | Identical under single numbering |
| Identical/Equivalent Standards: | ISO 13022:2012 |
| Organisation : |
| Indian Standards Refered In IS IS/ISO 13022 : 2012 : |
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| International Standards Refered In IS/ISO 13022 : 2012 |
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| IS/ISO 13022 : 2012 is Refered in following Indian Standards : | Standard contains no Cross Referenced Indian Standard. |