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Registry EUDAMED 42 FDA 510(k) incl. De Novo FDA PMA GUDID

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Risk class Class I 42 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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42 devices foundsorted by relevance

Manufacturer: CICHOSZ Spółka Komandytowa× Clear all

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Dakota Plus Double

CICHOSZ Spółka Komandytowa,Poland

Withdrawn Regimes: CE MDR, withdrawn Registry: EUDAMED Class:I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

CICHOSZ Spółka Komandytowa,Poland

Withdrawn Regimes: CE MDR, withdrawn Registry: EUDAMED Class:I

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Showing 41-42 of 42

deviCERTS Global Medical Device Regulatory Database

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Dakota Plus Double

Dakota Max