Identity
- Trade Name
- DRYSTAR DT 5.000I B EUDAMED
- Device Name
- Hard Copy Film EUDAMED
- Model / Reference
- ERRWB EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05414904014059 EUDAMED
- Basic UDI-DI
- 5414904273005XE EUDAMED
- Unit of Use DI
- 05414904224298 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 5.000i 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 70a27070-233f-4498-9343-d473ff8a1723 61 fields · synced Jun 18, 2026