Results for “Klinion® Kliniderm® Super fiber + Antimicrobial Polymer Technology™”

Name, manufacturer or identifier

Manufacturer (optional)

Filters

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

Country / market European Union (all) 4

More countries (1)

Germany 4

Risk class Class I Class IIa Class IIb 4 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

4 devices foundsorted by relevance

Clear all

DeviceDevice · Manufacturer · Authorizations Verified

Status

Regime

Registry

Class

Klinion® Kliniderm® Super fiber + Antimicrobial Polymer Technology™

Polaroid Therapeutics AG,Switzerland Group of variants

Active Regimes: CE MDR Registry: EUDAMED Class:IIb

Previous Next

Showing 1-4 of 4

deviCERTS Global Medical Device Regulatory Database

About [email protected]