Results for “BIONIKA DN, Implantátum behajtó, kézi, bordás”

Name, manufacturer or identifier

Manufacturer (optional)

Filters

Registry EUDAMED 6 FDA 510(k) incl. De Novo FDA PMA GUDID

Country / market European Union (all) 6

More countries (1)

Hungary 6

Risk class Class I 6 Class IIa Class IIb Class III Class II (US)

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)

Verified Verified only

Category (EMDN)

Browse by category

6 devices foundsorted by relevance

Clear all

DeviceDevice · Manufacturer · Authorizations Verified

Status

Regime

Registry

Class

BIONIKA DN, Implantátum behajtó, kézi, bordás

BIONIKA Medline Kft.,Hungary Group of variants

Active Regimes: CE MDR Registry: EUDAMED Class:I
BIONIKA DN, Implantátum behajtó, kézi, lamellás, bordás

BIONIKA Medline Kft.,Hungary Group of variants

Active Regimes: CE MDR Registry: EUDAMED Class:I

Previous Next

Showing 1-6 of 6

deviCERTS Global Medical Device Regulatory Database

About [email protected]

Results for “BIONIKA DN, Implantátum behajtó, kézi, bordás”

Category (EMDN)

BIONIKA DN, Implantátum behajtó, kézi, bordás

BIONIKA DN, Implantátum behajtó, kézi, lamellás, bordás