ONORM EN ISO 10993-12 : 2012
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
View Superseded by
BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 12: SAMPLE PREPARATION AND REFERENCE MATERIALS (ISO 10993-12:2012)
09-15-2021
01-12-2013
Der vorliegende Teil der ISO 10993 legt Anforderungen fest und gibt Anleitungen zu Verfahren, die bei der Probenvorbereitung und bei der Auswahl von Referenzmaterialien für die biologische Prüfung von Medizinprodukten nach einem oder mehreren Teilen der ISO 10993-Reihe zu befolgen sind.
| Committee |
TC 179
|
| DocumentType |
Standard
|
| PublisherName |
Osterreichisches Normungsinstitut/Austrian Standards
|
| Status |
Withdrawn
|
| SupersededBy |
| Standards | Relationship |
| I.S. EN ISO 10993-12:2012 | Identical |
| NF EN ISO 10993-12 : 2012 | Identical |
| NEN EN ISO 10993-12 : 2012 | Identical |
| SN EN ISO 10993-12 : 2012 | Identical |
| UNE-EN ISO 10993-12:2013 | Identical |
| DIN EN ISO 10993-12:2012-10 | Identical |
| EN ISO 10993-12:2012 | Identical |
| NBN EN ISO 10993-12 : 2012 | Identical |
| NS EN ISO 10993-12 : 2012 | Identical |
| UNI EN ISO 10993-12 : 2012 | Identical |
| ISO 10993-12:2012 | Identical |
| BS EN ISO 10993-12:2012 | Identical |
| OVE/ONORM EN 60601-1 : 2014 | MEDICAL ELECTRICAL EQUIPMENT - PART 1: GENERAL REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE (IEC 60601-1:2005 + COR.:2006 + COR.:2007 + A1:2012) |
| ISO 14971:2007 | Medical devices Application of risk management to medical devices |
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