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Oxford Unicompartmental Knee Phase 3replacement Anti-Static Cushion Pad

FDA UDI

Class I (US FDA UDI)

by Biomet Uk Ltd

Identity

Trade Name
OXFORD UNICOMPARTMENTAL KNEE PHASE 3REPLACEMENT ANTI-STATIC CUSHION PAD FDA UDI
Generic Name
Leg procedure positioner FDA UDI
Model / Reference
32-421713 FDA UDI

Identifiers

Catalog Number
32-421713 FDA UDI
Primary DI / UDI-DI
00880304652187 FDA UDI
FDA Product Code
CCX FDA UDI
GMDN Term
Leg procedure positioner FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.6820 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Leg procedure positioner

Oxford Unicompartmental Knee Phase 3replacement Anti-Static Cushion Pad by Biomet Uk Ltd — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Leg procedure positioner.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biomet Uk Ltd

Sources (1)

  • FDA UDI 14e70aba-fd72-4ef0-bfe0-992456d6ff28 34 fields · synced Jun 6, 2026