Identity
- Trade Name
- SOMER uterine elevat.forceps. S/S EUDAMED
- Device Name
- SOMER uterine elevat.forceps. S/S EUDAMED
- Model / Reference
- 7054723 EUDAMED
Identifiers
- Primary DI / UDI-DI
- G47270547230 EUDAMED
- Basic UDI-DI
- ++G4727054723VR EUDAMED
- EMDN Code
- L0509030299 UTERINE FORCEPS, REUSABLE - OTHER EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Germany EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
Yes
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
SOMER uterine elevat.forceps. S/S by HB Meditech (Pvt) Limited — 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 | ++G4727054723VR | Class I | Active |
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Manufacturer
- Manufacturer
- HB Meditech (Pvt) Limited
- EUDAMED SRN
- PK-MF-000024590
- Authorised Representative
- ANTEX MEDI SOLUTION DE-AR-000008078
Sources (1)
- EUDAMED 77d1e9f3-a675-4442-ad7b-1df55559bae1 61 fields · synced Jul 19, 2026