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The Active Implantable Medical Devices Regulations 1992
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- 1992 No. 3146
- Table of Contents
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SCHEDULES
Evaluation etc. of clinical data (corresponding to Annex 7 of the Directive)
Conditions relating to devices for special purposes (corresponding to Annex 6 of the Directive)
EC declaration of conformity procedure (corresponding to Annex 2 of the Directive) —
EC type—examination procedure (corresponding to Annex 3 of the Directive)
EC verification procedure (corresponding to Annex 4 of the Directive)
EC declaration of conformity to type procedure (corresponding to Annex 5 of the Directive) —
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