LP RING LOC ACETABULAR CUP 423676

GUDID 00880304372344

Biomet Orthopedics, LLC

Orthopaedic implant impactor, reusable

• Primary Device ID: 00880304372344
• NIH Device Record Key: 31ab4c7f-9e36-4ef2-ba64-8eacb19c9a8a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LP RING LOC ACETABULAR CUP
• Version Model Number: 423676
• Catalog Number: 423676
• 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: true
• 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	00880304372344 [Primary]

FDA Product Code

• HWA: IMPACTOR

Sterilization

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

[00880304372344]

Moist Heat or Steam Sterilization

[00880304372344]

Moist Heat or Steam Sterilization

[00880304372344]

Moist Heat or Steam Sterilization

[00880304372344]

Moist Heat or Steam Sterilization

[00880304372344]

Moist Heat or Steam Sterilization

[00880304372344]

Moist Heat or Steam Sterilization

[00880304372344]

Moist Heat or Steam Sterilization

[00880304372344]

Moist Heat or Steam Sterilization

[00880304372344]

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

On-Brand Devices [LP RING LOC ACETABULAR CUP]

• 00880304372368: 423678
• 00880304372351: 423677
• 00880304372344: 423676
• 00880304372320: 423674