Skip to content

Devices Categories Manufacturers Importers Certifiers Authorities Reps. Representatives

Results for “ReflexWear®”

Name, manufacturer or identifier

Manufacturer (optional)

Filters

Registry EUDAMED 43 FDA 510(k) FDA PMA GUDID

Country / market European Union (all) 43

More countries (1)

Denmark 43

Risk class Class I 43 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 Validated only

Category (EMDN)

Browse by category

43 devices foundsorted by relevance

Device · Manufacturer · Authorizations

ReflexWear® UDI-DI 05745000041060

Kilde & Co. ApS,Denmark Class I

Active CE MDR EUDAMED I
43 variants
- ReflexWear® 100011
- ReflexWear® 106123
- ReflexWear® 120012
- ReflexWear® 120013
- ReflexWear® 126122
- ReflexWear® 126123
- ReflexWear® 150011
- ReflexWear® 200011
- ReflexWear® 200012
- ReflexWear® 200014
- ReflexWear® 206122
- ReflexWear® 300011
- ReflexWear® 300012
- ReflexWear® 306121
- ReflexWear® 500013
- ReflexWear® 506121
- See all variants of this device

Showing 21-40 of 43

deviCERTS Global Medical Device Regulatory Database

About [email protected]

© 2026 deviCERTS — digitaly.site