Identity
- Device Name
- Albumina BM 100 / BM 200 EUDAMED
- Model / Reference
- 1-003-0200 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05902643961029 EUDAMED
- Basic UDI-DI
- 59026439BBCH0039V EUDAMED
- EMDN Code
- W01010201 ALBUMIN (CC) EUDAMED
Classification
- Device Class
- Class B EUDAMED
- Market of Registration
- Poland EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Microbial Substances
No
EUDAMED
Reagent
No
EUDAMED
Self Testing
No
EUDAMED
Near-Patient Testing
No
EUDAMED
Professional Testing
Yes
EUDAMED
Companion Diagnostics
No
EUDAMED
Surgical Instrument
No
EUDAMED
New Device
No
EUDAMED
Albumina BM 100 / BM 200 by BioMaxima Spółka Akcyjna — Class B — IVDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/IVDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDR | 59026439BBCH0039V | Class B | Active |
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Manufacturer
- Manufacturer
- BioMaxima Spółka Akcyjna
- EUDAMED SRN
- PL-MF-000039473
Sources (1)
- EUDAMED f1fb8108-43ec-415a-a355-4b063099a545 61 fields · synced Jun 18, 2026