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Attune

FDA UDI

Class II (US FDA UDI)

by Depuy (ireland)

Identity

Trade Name
ATTUNE FDA UDI
Generic Name
Knee femur stem/sleeve connector FDA UDI
Device Name
ATTUNE KNEE SYSTEM REVISION SLEEVE LIMB PRESERVATION SYSTEM FEMORAL ADAPTOR +0 MM FDA UDI
Model / Reference
1511-06-000 FDA UDI
Description
ATTUNE KNEE SYSTEM REVISION SLEEVE LIMB PRESERVATION SYSTEM FEMORAL ADAPTOR +0 MM FDA UDI

Identifiers

Catalog Number
151106000 FDA UDI
Primary DI / UDI-DI
10603295503408 FDA UDI
FDA Product Code
MBH FDA UDI
JWH FDA UDI
GMDN Term
Knee femur stem/sleeve connector FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3565 FDA UDI
888.3560 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
MRI Safety
MR Conditional FDA UDI

Category: Knee femur stem/sleeve connector

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

Similar devices

Also classified as Knee femur stem/sleeve connector.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Depuy (ireland)

Sources (1)

  • FDA UDI bad1b1d6-fcf1-41d9-b646-77d304cada5f 35 fields · synced May 30, 2026