Identity
- Trade Name
- DRYSTAR DT 10 B EUDAMED
- Device Name
- Hard Copy Film EUDAMED
- Model / Reference
- 51BCN EUDAMED51BGV EUDAMED51BDP EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05414904175187 EUDAMED05414904175620 EUDAMED05414904175194 EUDAMED
- Basic UDI-DI
- 5414904273005XE EUDAMED
- Unit of Use DI
- 05414904229897 EUDAMED05414904229811 EUDAMED05414904229873 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 10 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Agfa NV
- EUDAMED SRN
- BE-MF-000000571
Sources (3)
- EUDAMED 0ab46a24-53b2-450d-b4ba-6f0d0a75601b 61 fields · synced Sep 17, 2026
- EUDAMED 94405d82-2ab0-423f-9c65-d0a3c6bb6c6a 61 fields · synced May 17, 2026
- EUDAMED cca625d6-b568-49d1-81c0-c735953cc012 61 fields · synced May 17, 2026