Skip to content

Devices Categories Manufacturers Importers Certifiers Authorities Reps. Representatives

Results for “SenSura Mio Convex”

Name, manufacturer or identifier

Manufacturer (optional)

Filters

Registry EUDAMED 834 FDA 510(k) incl. De Novo FDA PMA GUDID 310

Country / market European Union (all) 659 United States 310

More countries (16)

Sweden 111 Italy 92 Austria 91 Netherlands 88 Germany 71 Liechtenstein 53 Norway 48 Denmark 44 Ireland 36 Finland 35 France 27 Poland 27 Belgium 18 Slovenia 9 Slovakia 8 Czechia 2

Risk class Class I 1,013 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

1,000+ devices foundsorted by relevance

DeviceDevice · Manufacturer · Authorizations Verified

Status

Regime

Registry

Class

SenSura Mio Convex

Coloplast A/S,Denmark Group of variants

Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:I
SenSura Mio Convex

Coloplast A/S,Denmark Group of variants

Active Regimes: CE MDR Registry: EUDAMED Class:I
SenSura Mio Convex Flip

Coloplast A/S,Denmark Group of variants

Active Regimes: CE MDR Registry: EUDAMED Class:I

deviCERTS Global Medical Device Regulatory Database

About [email protected]

© 2026 deviCERTS — digitaly.site