← Back to catalogue
P.f.c. Σ
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref 96-1411Model PFC SIGMA Tibial Insert Trial
Identity
- Trade Name
- P.F.C. Σ EUDAMEDP.F.C. SIGMA FDA UDI
- Generic Name
- Knee tibia prosthesis trial, reusable FDA UDI
- Device Name
- Tibial Insert Trial EUDAMEDP.F.C. SIGMA STABILIZED TIBIAL INSERT TRIAL SZ 1.5 10mm 61mm M/L 41mm A/P FDA UDI
- Model / Reference
- PFC SIGMA Tibial Insert Trial EUDAMED96-1411 EUDAMEDFDA UDI
- Description
- P.F.C. SIGMA STABILIZED TIBIAL INSERT TRIAL SZ 1.5 10mm 61mm M/L 41mm A/P FDA UDI
Identifiers
- Catalog Number
- 961411 FDA UDI
- Primary DI / UDI-DI
- 10603295237884 EUDAMEDFDA UDI
- Basic UDI-DI
- 0603295a001578Q EUDAMED
- Direct Marketing DI
- 10603295237884 EUDAMED
- FDA Product Code
- HWT FDA UDI
- EMDN Code
- L091199 ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER EUDAMED
- GMDN Term
- Knee tibia prosthesis trial, reusable FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass I FDA UDI
- Regulation Number
- 888.4800 FDA UDI
- Market of Registration
- Ireland EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
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
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
P.f.c. Σ by DePuy Ireland UC — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 0603295a001578Q | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- DePuy Ireland UC
- EUDAMED SRN
- IE-MF-000007377
Sources (2)
- EUDAMED 08cc6ede-4e9e-4c50-9f30-5b770a2d1321 61 fields · synced Jun 18, 2026
- FDA UDI 88c20240-9fcf-4cb3-809e-9266036b59f5 35 fields · synced May 30, 2026