Skip to content

Devices Categories Manufacturers Importers Certifiers Authorities Reps. Representatives

Results for “refleX”

Name, manufacturer or identifier

Manufacturer (optional)

Filters

Registry EUDAMED 484 FDA 510(k) 66 FDA PMA GUDID 569

Country / market European Union (all) 348 United States 634

More countries (13)

Italy 134 Germany 55 Denmark 43 Netherlands 40 Türkiye 38 Poland 28 France 25 Austria 9 Belgium 8 Sweden 3 Bulgaria 1 Finland 1 Ireland 1

Risk class Class I 844 Class IIa 14 Class IIb 16 Class III Class II (US) 187

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) 3 Not classified (FDA)

Verified Validated only

Category (EMDN)

Browse by category

1,000+ devices foundsorted by relevance

Device · Manufacturer · Authorizations

Varilite Reflex UDI-DI 00040818920619

Cascade Designs, Inc.,United States Class I

Active CE MDR EUDAMEDGUDID I
41 variants
- Varilite Reflex 73500112122
- Varilite Reflex 73500114143
- Varilite Reflex 73500114163
- Varilite Reflex 73500114202
- Varilite Reflex 73500114203
- Varilite Reflex 73500115153
- Varilite Reflex 73500116142
- Varilite Reflex 73500116162
- Varilite Reflex 73500116182
- Varilite Reflex 73500117173
- Varilite Reflex 73500117193
- Varilite Reflex 73500118182
- Varilite Reflex 73500118183
- Varilite Reflex 73500118202
- Varilite Reflex 73500118203
- Varilite Reflex 73500120162
- See all variants of this device

deviCERTS Global Medical Device Regulatory Database

About [email protected]

© 2026 deviCERTS — digitaly.site