00-5842-026-10

GUDID 00889024633841

Zimmer, Inc.

Unicondylar knee insert

• Primary Device ID: 00889024633841
• NIH Device Record Key: 10bea07d-0ae2-4fa7-b82b-75b8ee8f2561
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 5842-26-10
• Catalog Number: 00-5842-026-10
• Company DUNS: 056038268
• Company Name: Zimmer, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• 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)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com

Device Dimensions

• Device Size Text, specify: 0
• Height: 10 Millimeter
• Device Size Text, specify: 0
• Height: 10 Millimeter
• Device Size Text, specify: 0
• Height: 10 Millimeter
• Device Size Text, specify: 0
• Height: 10 Millimeter
• Device Size Text, specify: 0
• Height: 10 Millimeter
• Device Size Text, specify: 0
• Height: 10 Millimeter
• Device Size Text, specify: 0
• Height: 10 Millimeter
• Device Size Text, specify: 0
• Height: 10 Millimeter
• Device Size Text, specify: 0
• Height: 10 Millimeter
• Device Size Text, specify: 0
• Height: 10 Millimeter
• Device Size Text, specify: 0
• Height: 10 Millimeter
• Device Size Text, specify: 0
• Height: 10 Millimeter
• Device Size Text, specify: 0
• Height: 10 Millimeter
• Device Size Text, specify: 0
• Height: 10 Millimeter
• Device Size Text, specify: 0
• Height: 10 Millimeter
• Device Size Text, specify: 0
• Height: 10 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00889024633841 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K033363

FDA Product Code

• HSX: PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-03-07
• Device Publish Date: 2022-02-25

Devices Manufactured by Zimmer, Inc.

• 00889024681897 - Alliance: 2025-08-14
• 00889024681903 - Alliance: 2025-08-14
• 00889024681910 - Comprehensive: 2025-08-14
• 00889024681927 - Alliance: 2025-08-14
• 00889024681934 - Comprehensive: 2025-08-14
• 00889024681941 - Comprehensive: 2025-08-14
• 00889024681958 - Comprehensive: 2025-08-14
• 00889024681965 - Comprehensive: 2025-08-14