Identity
- Model / Reference
- 15110001 EUDAMED15490050 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05060498302302 EUDAMED
- Basic UDI-DI
- 50560383NeuraxialAcc2T EUDAMED
- Unit of Use DI
- 05060498307710 EUDAMED
- EMDN Code
- A019001 BLUNT NEEDLES EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Germany 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
Yes
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
15490050 by GBUK Group — 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 | 50560383NeuraxialAcc2T | Class I | Active |
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Manufacturer
- Manufacturer
- GBUK Group
- EUDAMED SRN
- GB-MF-000002238
- Authorised Representative
- Qualrep Services B.V. NL-AR-000000537
Sources (1)
- EUDAMED d36390eb-5c1a-4271-b0b4-925c0c8c2b96 61 fields · synced Jul 14, 2026