Skip to content

Devices Categories Manufacturers Importers Certifiers Authorities Reps. Representatives

Results for “URGOTUL”

Name, manufacturer or identifier

Manufacturer (optional)

Filters

Registry EUDAMED 122 FDA 510(k) incl. De Novo 2 FDA PMA GUDID 43

Country / market European Union (all) 103 United States 45

More countries (8)

Germany 46 Spain 20 Northern Ireland 17 France 14 Netherlands 11 Poland 8 Italy 4 Türkiye 2

Risk class Class I 37 Class IIa Class IIb 122 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) 2 Not classified (FDA)

Verified Verified only

Category (EMDN)

Browse by category

167 devices foundsorted by relevance

DeviceDevice · Manufacturer · Authorizations Verified

Status

Regime

Registry

Class

Urgotul

Laboratoires Urgo,France Group of variants

Active Regimes: CE MDR Registry: EUDAMED Class:IIb
URGOTÜL Flex

Laboratoires Urgo,France

Active Regimes: CE MDR Registry: EUDAMED Class:IIb
URGOTUL Duo

Laboratoires Urgo,France

Active Regimes: CE MDR Registry: EUDAMED Class:IIb

Showing 161-167 of 167

deviCERTS Global Medical Device Regulatory Database

About [email protected]

© 2026 deviCERTS — digitaly.site