Oxford Unicompartmental Knee Phase 3cement Removal Chisel

FDA UDI

Class I (US FDA UDI)

by Biomet Uk Ltd

Identity

Trade Name: OXFORD UNICOMPARTMENTAL KNEE PHASE 3CEMENT REMOVAL CHISEL FDA UDI
Generic Name: Orthopaedic chisel FDA UDI
Model / Reference: 32-420804 FDA UDI

Identifiers

Catalog Number: 32-420804 FDA UDI
Primary DI / UDI-DI: 05019279490042 FDA UDI
FDA Product Code: LXH FDA UDI
GMDN Term: Orthopaedic chisel 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

Yes

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: Orthopaedic chisel

Oxford Unicompartmental Knee Phase 3cement Removal Chisel by Biomet Uk Ltd — Class I — 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 I	Pending data

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Manufacturer

Manufacturer: Biomet Uk Ltd

Sources (1)

FDA UDI b9243cb7-b70f-4379-8dbd-e9f2ba89cb05 34 fields · synced Jun 8, 2026