Identity
- Device Name
- MAXIMUS X EUDAMED
- Model / Reference
- 30010300 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 07290016586367 EUDAMED
- Basic UDI-DI
- B-07290016586367 EUDAMED
- EMDN Code
- Z12040280,Z12040299 EUDAMED
Classification
- Device Class
- Class IIb EUDAMED
- Market of Registration
- Belgium EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Maximus X by Pollogen Ltd — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-07290016586367 | Class IIb | Active |
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Manufacturer
- Manufacturer
- Pollogen Ltd
- EUDAMED SRN
- IL-MF-000031034
- Authorised Representative
- Obelis s.a. BE-AR-000000106
Sources (1)
- EUDAMED bd730e5e-4b4c-41db-9db3-1692f5ac3a51 61 fields · synced Jun 20, 2026