Identity
- Device Name
- Splinter forcep EUDAMED
- Model / Reference
- Splinter forcep EUDAMED
Identifiers
- Primary DI / UDI-DI
- 111823008317 EUDAMED
- Basic UDI-DI
- PP12633SPLINTERFORCEP20 EUDAMED
- Direct Marketing DI
- 111823008317 EUDAMED
- EMDN Code
- L03130403 SPLINTER FORCEPS, REUSABLE EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Bulgaria 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 by Qureshi Manufacturing Corporation — 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 | PP12633SPLINTERFORCEP20 | Class I | Active |
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Manufacturer
- Manufacturer
- Qureshi Manufacturing Corporation
- EUDAMED SRN
- PK-MF-000024744
- Authorised Representative
- AF Pharma Service Europe SL ES-AR-000018076
Sources (1)
- EUDAMED 134db784-0575-47e5-a671-2856969159da 61 fields · synced Jun 18, 2026