Identity
- Device Name
- HWS Cervikal 040.09.1000 Mul. EUDAMED
- Model / Reference
- 9ANC-1001 EUDAMED
Identifiers
- Primary DI / UDI-DI
- D-9ANC-1001GS EUDAMED
- Basic UDI-DI
- B-9ANC-1001GS EUDAMED
- EMDN Code
- Z121301 PERCUTANEOUS DISCECTOMY EQUIPMENT EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Germany EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
Yes
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
HWS Cervikal 040.09.1000 Mul. by Blazejewski MEDI-TECH 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-9ANC-1001GS | Class IIa | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Blazejewski MEDI-TECH GmbH
- EUDAMED SRN
- DE-MF-000005467
Sources (1)
- EUDAMED f0c82762-539f-43ff-8a74-1397e39ef099 61 fields · synced Jun 18, 2026