Oxford Partial Knee SystemFemoral Impactor 32-420127

GUDID 05019279477333

Biomet Uk Ltd

Orthopaedic implant impactor, reusable

• Primary Device ID: 05019279477333
• NIH Device Record Key: 3befd5e5-60ce-441d-9eb6-0ef233cad330
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Oxford Partial Knee SystemFemoral Impactor
• Version Model Number: 32-420127
• Catalog Number: 32-420127
• Company DUNS: 219322575
• Company Name: Biomet Uk Ltd
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	05019279477333 [Primary]

FDA Product Code

• HWA: IMPACTOR

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[05019279477333]

Moist Heat or Steam Sterilization

[05019279477333]

Moist Heat or Steam Sterilization

[05019279477333]

Moist Heat or Steam Sterilization

[05019279477333]

Moist Heat or Steam Sterilization

[05019279477333]

Moist Heat or Steam Sterilization

[05019279477333]

Moist Heat or Steam Sterilization

[05019279477333]

Moist Heat or Steam Sterilization

[05019279477333]

Moist Heat or Steam Sterilization

[05019279477333]

Moist Heat or Steam Sterilization

[05019279477333]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2026-02-09
• Device Publish Date: 2020-05-23

Devices Manufactured by Biomet Uk Ltd

• 05019279477333 - Oxford Partial Knee SystemFemoral Impactor: 2026-02-09
• 05019279477333 - Oxford Partial Knee SystemFemoral Impactor: 2026-02-09
• 05019279905638 - OXFORD UNICOMPARTMENTAL KNEE PHASE 3TIBIAL IMPACTOR: 2026-02-09
• 05019279439935 - Oxford® Partial Knee System: 2025-05-23
• 05019279439942 - Oxford® Partial Knee System: 2025-05-23
• 05019279439959 - Oxford® Partial Knee System: 2025-05-23
• 00880304525672 - Oxford® Partial Knee System: 2025-01-20
• 00887868259050 - Oxford® Partial Knee System: 2025-01-20
• 00887868354694 - Oxford® Partial Knee System: 2025-01-20