NA 176
DIN Standards Committee Health Technologies
DIN EN 13060 [Withdrawn] references following documents:
| Document number | Edition | Title |
|---|---|---|
| EN ISO 14937 | 2009-10 | 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 (ISO 14937:2009) More |
| EN ISO 228-1 | 2003-02 | Pipe threads where pressure-tight joints are not made on the threads - Part 1: Dimensions, tolerances and designation (ISO 228-1:2000) More |
| EN 60529 | 1991-10 | Degrees of protection provided by enclosures (IP code) (IEC 60529:1989) More |
| EN 61010-1 | 2001-03 | Safety requirements for electrical equipment for measurement, control and laboratory use - Part 1: General requirements (IEC 61010-1:2001) More |
| EN 61010-2-041 | 1996-03 | Safety requirements for electrical equipment for measurement, control and laboratory use - Part 2-041: Particular requirements for autoclaves using steam for the treatment of medical materials, and for laboratory processes (IEC 61010-2-041:1996) More |
| EN 61326 | 1997-04 | Electrical equipment for measurement, control and laboratory use - EMC requirements (IEC 61326:1997) More |
| EN ISO 10993-14 | 2009-04 | Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001) More |
| EN ISO 10993-5 | 2009-06 | Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009) More |
| EN ISO 10993-7 | 2008-10 | Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:2008) More |
| EN ISO 10993-7/AC | 2009-11 | Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals; Technical Corrigendum 1 (ISO 10993-7:2008/Cor 1:2009) More |
