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Results for “COLUMBUS REVISION”

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Registry EUDAMED 415 FDA 510(k) incl. De Novo 4 FDA PMA GUDID 733

Country / market European Union (all) 232 United States 737

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Germany 232

Risk class Class I 151 Class IIa 208 Class IIb Class III Class II (US) 388

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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747 devices foundsorted by relevance

DeviceDevice · Manufacturer · Authorizations Verified

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Columbus Revision

Aesculap AG,Germany Group of variants

Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:IIa
Columbus Revision

Aesculap AG,Germany

Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:I
Columbus Revision F

Aesculap AG,Germany

Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:I
Columbus Revision F

Aesculap AG,Germany

Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:IIa

Showing 301-320 of 747

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