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BS EN ISO 11137-1:2015 Sterilization of health care products. Radiation - Requirements for development, validation and routine control of a sterilization process for medical devices >
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BS EN ISO 11137-1:2015 Sterilization of health care products. Radiation - Requirements for development, validation and routine control of a sterilization process for medical devices, 2015
- Contents Page
- Foreword
- Table — Correlation between normative references and dated EN and ISO standards
- Endorsement notice
- Annex ZA (informative) Relationship between this European Standard and the Essential Requirements of EU Directive 90/385/EEC on active implantable medical devices
- Table ZA.1 — Correspondence between this European Standard and Directive 90/385/EEC
- Annex ZB (informative) Relationship between this European Standard and the Essential Requirements of EU Directive 93/42/EEC on medical devices
- Table ZB.1 — Correspondence between this European Standard and Directive 93/42/EEC
- Annex ZC (informative) Relationship between this European Standard and the Essential Requirements of EU Directive 98/79/EC on in vitro diagnostic medical devices
- Table ZC.1 — Correspondence between this European Standard and Directive 98/79/EC
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