Oxford Partial Knee System

FDA UDI

Class III (US FDA UDI)

by Biomet Uk Ltd

Identity

Trade Name: Oxford Partial Knee System FDA UDI
Generic Name: Knee tibia prosthesis trial, reusable FDA UDI
Device Name: Left Medial Trial Tibial Tray FDA UDI
Model / Reference: 32-420360 FDA UDI
Description: Left Medial Trial Tibial Tray FDA UDI

Identifiers

Catalog Number: 32-420360 FDA UDI
Primary DI / UDI-DI: 05019279482993 FDA UDI
PMA Number: P010014 FDA UDI
FDA Product Code: NRA FDA UDI
GMDN Term: Knee tibia prosthesis trial, reusable FDA UDI

Classification

Device Class: Class III FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

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

Yes

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

MRI Safety

MR Conditional FDA UDI

Dimensions & Sizes

Size: Length — 34 Millimeter FDA UDI
Length — 53 Millimeter FDA UDI

Category: Knee tibia prosthesis trial, reusable

Oxford Partial Knee System by Biomet Uk Ltd — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

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 III	Pending data

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Manufacturer

Manufacturer: Biomet Uk Ltd

Sources (1)

FDA UDI 99d5d25b-c69f-46da-bd26-95a57ffbe24b 37 fields · synced Jun 6, 2026