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Results for “RapidFor™”

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Registry EUDAMED 508 FDA 510(k) incl. De Novo FDA PMA GUDID

Country / market European Union (all) 120

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Türkiye 388 Germany 120

Risk class Class I Class IIa Class IIb Class III Class II (US)

More classes (11)

Class A Class B 72 Class C 36 Class D IVD General 398 IVD Annex II List A IVD Annex II List B IVD for self-testing 2 Active implantable (AIMDD) Unclassified (FDA) Not classified (FDA)

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508 devices foundsorted by relevance

DeviceDevice · Manufacturer · Authorizations Verified

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RapidFor™

Vitrosens Biotechnology Inc.,Türkiye Group of variants

Active Regimes: CE IVDR CE IVDD Registry: EUDAMED Class:B
RapidFor™

Vitrosens Biotechnology Inc.,Türkiye Group of variants

Active Regimes: CE IVDR CE IVDD Registry: EUDAMED Class:IVD General
RapidFor™

Vitrosens Biotechnology Inc.,Türkiye Group of variants

Active Regimes: CE IVDR CE IVDD Registry: EUDAMED Class:C

Showing 141-160 of 508

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