← Back to catalogue
Inj1-A2-07-4-23-230
EUDAMEDClass IIa (EU MDR)
Ref 70100146671Model INJ1-A2-07-4-23-230
Identity
- Trade Name
- INJ1-A2-07-4-23-230 EUDAMED
- Device Name
- INJ1-Series EUDAMED
- Model / Reference
- INJ1-A2-07-4-23-230 EUDAMED70100146671 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04044503053817 EUDAMED
- Basic UDI-DI
- B-04044503053817 EUDAMED
- EMDN Code
- G03020101 DIGESTIVE ENDOSCOPY, SINGLE-LUMEN NEEDLES EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Germany EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Inj1-A2-07-4-23-230 by FUJIFILM medwork GmbH — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-04044503053817 | Class IIa | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- FUJIFILM medwork GmbH
- EUDAMED SRN
- DE-MF-000008444
Sources (1)
- EUDAMED c864a19d-81fd-43a1-bb97-b3d131568105 61 fields · synced Jul 15, 2026