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Drystar Dt 5.000i B
EUDAMEDClass I (EU MDR)
Ref ERRU6Ref ERRT4Ref ERRV8
by Agfa NV
Identity
- Trade Name
- DRYSTAR DT 5.000I B EUDAMED
- Device Name
- Hard Copy Film EUDAMED
- Model / Reference
- ERRU6 EUDAMEDERRT4 EUDAMEDERRV8 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05414904014073 EUDAMED05414904014080 EUDAMED05414904014066 EUDAMED
- Basic UDI-DI
- 5414904273005XE EUDAMED
- Unit of Use DI
- 05414904224335 EUDAMED05414904224359 EUDAMED05414904224311 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 (3)
- EUDAMED e3076f2e-0f25-4c37-8dc5-1175de93ca02 61 fields · synced Jul 18, 2026
- EUDAMED 09e68919-b41a-4d81-8bcb-baeb64cbe5f4 61 fields · synced May 17, 2026
- EUDAMED bca8d056-b814-459f-859e-f87de4dfa203 61 fields · synced May 17, 2026