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Assess and designate Notified Bodies - TOPRA

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MEDDEVs<br />

2.1 Scope, field of application, definition<br />

2.2 Essential requirements<br />

2.4 Classification of Medical Devices<br />

2.5 Conformity assessment procedure<br />

– General rules<br />

– Conformity assessment for particular groups of products<br />

2.7 Clinical investigation, clinical evaluation<br />

2.10 <strong>Notified</strong> bodies<br />

2.11 Products using materials of biological origin<br />

2.12 Market surveillance<br />

2.13 Transitional period<br />

2.14 IVD<br />

2.15 Other guidance

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