Triathlon

FDA UDI

Class II (US FDA UDI)

by Howmedica Osteonics Corp.

Identity

Trade Name: Triathlon FDA UDI
Generic Name: Metal-backed patella prosthesis FDA UDI
Device Name: Metal Backed Patella FDA UDI
Model / Reference: 5554-L-401 FDA UDI
Description: Metal Backed Patella FDA UDI

Identifiers

Catalog Number: 5554-L-401 FDA UDI
Primary DI / UDI-DI: 07613327049923 FDA UDI
FDA Product Code: JWH FDA UDI
MBH FDA UDI
GMDN Term: Metal-backed patella prosthesis FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3560 FDA UDI
888.3565 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

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Metal-backed patella prosthesis

Triathlon by Howmedica Osteonics Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Howmedica Osteonics Corp.

Sources (1)

FDA UDI 614c16da-c48b-43e6-be8e-162fd1c08a42 35 fields · synced Jun 8, 2026