Identity
- Device Name
- ENT EUDAMED
- Model / Reference
- F5-268 EUDAMED
Identifiers
- Primary DI / UDI-DI
- +G742F52680K EUDAMED
- Basic UDI-DI
- ++G742ENTUK EUDAMED
- EMDN Code
- L03130403 SPLINTER FORCEPS, REUSABLE 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
Ent by Fairmount Industries Pvt Ltd — 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 | ++G742ENTUK | Class I | Active |
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Manufacturer
- Manufacturer
- Fairmount Industries Pvt Ltd
- EUDAMED SRN
- PK-MF-000044972
- Authorised Representative
- Maxcert Ltd XI-AR-000044423
Sources (1)
- EUDAMED a5e83cdc-5da8-4dda-9f6d-e8c6e90e4e49 61 fields · synced Jun 20, 2026