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Tri-Lock Gription

FDA UDI

Class III (US FDA UDI)

by Depuy Orthopaedics, Inc.

Identity

Trade Name
TRI-LOCK GRIPTION FDA UDI
Generic Name
Coated femoral stem prosthesis, one-piece FDA UDI
Device Name
TRI-LOCK BPS FEMORAL STEM 12/14 TAPER TRI-LOCK BPS W/GRIPTION SIZE 10 STD 115mm FDA UDI
Model / Reference
1012-04-100 FDA UDI
Description
TRI-LOCK BPS FEMORAL STEM 12/14 TAPER TRI-LOCK BPS W/GRIPTION SIZE 10 STD 115mm FDA UDI

Identifiers

Catalog Number
101204100 FDA UDI
Primary DI / UDI-DI
10603295000815 FDA UDI
FDA Product Code
MRA FDA UDI
LPH FDA UDI
LZO FDA UDI
GMDN Term
Coated femoral stem prosthesis, one-piece FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
888.3358 FDA UDI
888.3353 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Coated femoral stem prosthesis, one-piece

Tri-Lock Gription by Depuy Orthopaedics, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Coated femoral stem prosthesis, one-piece.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Depuy Orthopaedics, Inc.

Sources (1)

  • FDA UDI 9921fa0a-412e-4cc4-9647-1b76b4d01474 35 fields · synced Jun 7, 2026