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Registry EUDAMED 23 FDA 510(k) incl. De Novo FDA PMA GUDID

Country / market European Union (all) 23

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Germany 23

Risk class Class I 23 Class IIa 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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23 devices foundsorted by relevance

Manufacturer: Wieth Medical Systems e.K.× Clear all

DeviceDevice · Manufacturer · Authorizations Verified

Status

Regime

Registry

Class

Curvlight Pro

Wieth Medical Systems e.K.,Germany

Withdrawn Regimes: CE MDR, withdrawn Registry: EUDAMED Class:I
Curvlight Air

Wieth Medical Systems e.K.,Germany

Withdrawn Regimes: CE MDR, withdrawn Registry: EUDAMED Class:I
DELIGHT5.0

Wieth Medical Systems e.K.,Germany

Withdrawn Regimes: CE MDR, withdrawn Registry: EUDAMED Class:I

Showing 21-23 of 23

deviCERTS Global Medical Device Regulatory Database

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