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Results for “Lichthärtendes Material zur Herstellung von Otoplastiken.”

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Registry EUDAMED 96 FDA 510(k) incl. De Novo FDA PMA GUDID

Country / market European Union (all) 96

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Germany 96

Risk class Class I Class IIa 96 Class IIb Class III Class II (US)

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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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96 devices foundsorted by relevance

DeviceDevice · Manufacturer · Authorizations Verified

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Lichthärtendes Material zur Herstellung von Otoplastiken.

Dreve Otoplastik GmbH,Germany Group of variants

Active Regimes: CE MDR Registry: EUDAMED Class:IIa
Lichthärtendes Material zur Herstellung von Otoplastiken mittels 3D-Druck-Verfahren.

Dreve Otoplastik GmbH,Germany Group of variants

Active Regimes: CE MDR Registry: EUDAMED Class:IIa

Showing 41-60 of 96

deviCERTS Global Medical Device Regulatory Database

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