Skip to content

Devices Categories Manufacturers Importers Certifiers Authorities Reps. Representatives

Results for “MAGIK_DETE”

Name, manufacturer or identifier

Manufacturer (optional)

Filters

Registry EUDAMED 14 FDA 510(k) FDA PMA GUDID

Country / market European Union (all) 14

More countries (1)

France 14

Risk class Class I 14 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

14 devices foundsorted by relevance

Device · Manufacturer · Authorizations

Magik_dete UDI-DI 03376122307172

Podowell,France Class I

Active CE MDR EUDAMED I
14 variants
- Magik_dete MAGIK_DETE-1100-P36
- Magik_dete MAGIK_DETE-1100-P37
- Magik_dete MAGIK_DETE-1100-P38
- Magik_dete MAGIK_DETE-1100-P39
- Magik_dete MAGIK_DETE-1100-P40
- Magik_dete MAGIK_DETE-1100-P41
- Magik_dete MAGIK_DETE-1100-P42
- Magik_dete MAGIK_DETE-3500-P36
- Magik_dete MAGIK_DETE-3500-P38
- Magik_dete MAGIK_DETE-3500-P39
- Magik_dete MAGIK_DETE-3500-P40
- Magik_dete MAGIK_DETE-3500-P41
- Magik_dete MAGIK_DETE-3500-P42

Previous Next

Showing 1-14 of 14

deviCERTS Global Medical Device Regulatory Database

About [email protected]

© 2026 deviCERTS — digitaly.site