Attune

FDA UDI

Class I (US FDA UDI)

by Depuy (ireland)

Identity

Trade Name: ATTUNE FDA UDI
Generic Name: Knee femur prosthesis trial, reusable FDA UDI
Device Name: ATTUNE KNEE SYSTEM REVISION FEMORAL BOX TRIAL LEFT SIZE 4 FDA UDI
Model / Reference: 2504-40-124 FDA UDI
Description: ATTUNE KNEE SYSTEM REVISION FEMORAL BOX TRIAL LEFT SIZE 4 FDA UDI

Identifiers

Catalog Number: 250440124 FDA UDI
Primary DI / UDI-DI: 10603295442554 FDA UDI
FDA Product Code: LXH FDA UDI
GMDN Term: Knee femur prosthesis trial, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 888.4540 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Knee femur prosthesis trial, reusable

Attune by Depuy (ireland) — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Knee femur prosthesis trial, reusable.

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OSS™ — Biomet Orthopedics, Inc. · Class II
VANGUARD 360 INSTRUMENT — Biomet Orthopedics, Inc. · Class II
VANGUARD(TM) PS FEMORAL TRIAL — Biomet Orthopedics, Inc. · Class II
Natural-Knee® — Zimmer, Inc. · Class II
NexGen® — Zimmer, Inc. · Class II
LOSPA Knee System — Corentec Co., Ltd · Class II
Persona® — Zimmer, Inc. · Class II

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 I	Pending data

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Manufacturer

Manufacturer: Depuy (ireland)

Sources (1)

FDA UDI 356161c3-ffc8-4da1-8e4b-8e589b45c8c1 35 fields · synced Jun 8, 2026