Identity
- Trade Name
- DRYSTAR DT 5 B EUDAMED
- Device Name
- Hard Copy Film EUDAMED
- Model / Reference
- 51BOB EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05414904175699 EUDAMED
- Basic UDI-DI
- 5414904273005XE EUDAMED
- Unit of Use DI
- 05414904229675 EUDAMED
- EMDN Code
- Z130106 DRY THERMAL PRINTER X-RAY FILMS EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Belgium EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Drystar Dt 5 B by Agfa NV — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 5414904273005XE | Class I | Active |
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Manufacturer
- Manufacturer
- Agfa NV
- EUDAMED SRN
- BE-MF-000000571
Sources (1)
- EUDAMED 52034dba-64c3-4938-b008-75e3c9bd05a8 61 fields · synced Jun 18, 2026