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Pinnacle Gription Tf
EUDAMEDFDA UDIClass I (EU MDR)
Ref 2217-00-262Model Pinnacle Buttress Trial
Identity
- Trade Name
- PINNACLE GRIPTION TF EUDAMEDFDA UDI
- Generic Name
- Acetabulum prosthesis trial, prefabricated, reusable FDA UDI
- Device Name
- Buttress Trial EUDAMEDPINNACLE GRIPTION TF BUTTRESS TRIAL 62L FDA UDI
- Model / Reference
- Pinnacle Buttress Trial EUDAMED2217-00-262 EUDAMEDFDA UDI
- Description
- PINNACLE GRIPTION TF BUTTRESS TRIAL 62L FDA UDI
Identifiers
- Catalog Number
- 221700262 FDA UDI
- Primary DI / UDI-DI
- 10603295097433 EUDAMEDFDA UDI
- Basic UDI-DI
- 0603295a004959F EUDAMED
- Direct Marketing DI
- 10603295097433 EUDAMED
- FDA Product Code
- HWT FDA UDI
- EMDN Code
- L091199 ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER EUDAMED
- GMDN Term
- Acetabulum prosthesis trial, prefabricated, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA 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
Yes
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
Pinnacle Gription Tf by DePuy Ireland UC — Class I — 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 | 0603295a004959F | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- DePuy Ireland UC
- EUDAMED SRN
- IE-MF-000007377
Sources (2)
- EUDAMED 1600abb7-fc39-430c-807e-19b0109d8b74 61 fields · synced Jul 15, 2026
- FDA UDI 401d88f4-957e-4ef2-8fa2-0c9234997f07 35 fields · synced May 29, 2026