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Results for “BICONTACT S”

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Registry EUDAMED 52 FDA 510(k) incl. De Novo 2 FDA PMA GUDID

Country / market European Union (all) 52 United States 2

More countries (1)

Germany 52

Risk class Class I 50 Class IIa 2 Class IIb Class III Class II (US) 2

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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54 devices foundsorted by relevance

DeviceDevice · Manufacturer · Authorizations Verified

Status

Regime

Registry

Class

Bicontact S

Aesculap AG,Germany Group of variants

Active Regimes: CE MDR Registry: EUDAMED Class:I
Bicontact S/H

Aesculap AG,Germany

Active Regimes: CE MDR Registry: EUDAMED Class:IIa
Bicontact Sd

Aesculap AG,Germany

Active Regimes: CE MDR Registry: EUDAMED Class:I

Showing 41-54 of 54

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