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Results for “VITA AMBRIA®”

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Registry EUDAMED 79 FDA 510(k) incl. De Novo FDA PMA GUDID 73

Country / market European Union (all) 79 United States 73

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Germany 79

Risk class Class I Class IIa 79 Class IIb Class III Class II (US) 1

More classes (11)

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

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80 devices foundsorted by relevance

DeviceDevice · Manufacturer · Authorizations Verified

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Vita Ambria®

VITA Zahnfabrik H. Rauter GmbH & Co. KG,Germany Group of variants

Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:IIa
Vita Ambria LAMSKC1

Vita - Zahnfabrik H. Rauter Gesellschaft mit beschränkter Haftung & Co Kommanditgesellschaft,FDA registration: United States

None Registry: GUDID Class:II
Vita Ambria® Cad

VITA Zahnfabrik H. Rauter GmbH & Co. KG,Germany Group of variants

Active Regimes: CE MDR Registry: EUDAMED Class:IIa

Showing 61-80 of 80

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