Identity
- Trade Name
- Splinter Forcep Stieglitz EUDAMED
- Device Name
- Splinter Forcep Stieglitz EUDAMED
- Model / Reference
- 590 EUDAMED
Identifiers
- Primary DI / UDI-DI
- G5485900 EUDAMED
- Basic UDI-DI
- ++G548590NN EUDAMED
- EMDN Code
- L03130403 SPLINTER FORCEPS, REUSABLE EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Italy 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
Splinter Forcep Stieglitz by Prilanta Surgical — 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 | ++G548590NN | Class I | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Prilanta Surgical
- EUDAMED SRN
- PK-MF-000038228
- Authorised Representative
- ANTEX MEDI SOLUTION DE-AR-000008078
Sources (1)
- EUDAMED b8080404-0bdd-4807-bfb8-dd4bc2d2b11c 61 fields · synced Jun 17, 2026