← Back to catalogue

Pinnacle Gription Tf

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 2217-10-154Model PINNACLE GRIPTION Hip Augment Trial

by DePuy Ireland UC

Identity

Trade Name
PINNACLE GRIPTION TF EUDAMEDFDA UDI
Generic Name
Acetabulum prosthesis trial, prefabricated, reusable FDA UDI
Device Name
Hip Augment Trial EUDAMED
PINNACLE GRIPTION TF AUGMENT TRIAL 10 X 54/56 FDA UDI
Model / Reference
PINNACLE GRIPTION Hip Augment Trial EUDAMED
2217-10-154 EUDAMEDFDA UDI
Description
PINNACLE GRIPTION TF AUGMENT TRIAL 10 X 54/56 FDA UDI

Identifiers

Catalog Number
221710154 FDA UDI
Primary DI / UDI-DI
10603295098409 EUDAMEDFDA UDI
Basic UDI-DI
0603295a001338A EUDAMED
Direct Marketing DI
10603295098409 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 IIa EUDAMED
Class 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Pinnacle Gription Tf 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

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 2b9bffd9-f58f-4f75-a919-50924be3a96f 61 fields · synced Jun 18, 2026
  • FDA UDI 8d11177e-e75f-436b-9e29-bc0a5a02e5af 35 fields · synced May 30, 2026