IMPACTOR TIP 35-463128

GUDID 00880304360242

Biomet Orthopedics, LLC

Orthopaedic implant impactor, reusable

• Primary Device ID: 00880304360242
• NIH Device Record Key: 26d12d13-2ca7-4c86-85e4-883ae49d28c8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: IMPACTOR TIP
• Version Model Number: 35-463128
• Catalog Number: 35-463128
• Company DUNS: 129278169
• Company Name: Biomet Orthopedics, LLC
• 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
• 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	00880304360242 [Primary]

FDA Product Code

• HWA: IMPACTOR

Sterilization

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

[00880304360242]

Moist Heat or Steam Sterilization

[00880304360242]

Moist Heat or Steam Sterilization

[00880304360242]

Moist Heat or Steam Sterilization

[00880304360242]

Moist Heat or Steam Sterilization

[00880304360242]

Moist Heat or Steam Sterilization

[00880304360242]

Moist Heat or Steam Sterilization

[00880304360242]

Moist Heat or Steam Sterilization

[00880304360242]

Moist Heat or Steam Sterilization

[00880304360242]

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 Orthopedics, LLC

• 00880304360242 - IMPACTOR TIP: 2026-02-09
• 00880304360242 - IMPACTOR TIP: 2026-02-09
• 00880304371828 - LINER IMPACTOR PLATE HEAD: 2026-02-09
• 00880304371897 - LINER IMPACTOR PLATE: 2026-02-09
• 00880304371903 - LINER IMPACTOR PLATE: 2026-02-09
• 00880304372320 - LP RING LOC ACETABULAR CUP: 2026-02-09
• 00880304372344 - LP RING LOC ACETABULAR CUP: 2026-02-09
• 00880304372351 - LP RING LOC ACETABULAR CUP: 2026-02-09
• 00880304372368 - LP RING LOC ACETABULAR CUP: 2026-02-09