00-1142-001-25

GUDID 00889024024694

Zimmer, Inc.

Orthopaedic bone wire

• Primary Device ID: 00889024024694
• NIH Device Record Key: 5f3a08ff-cf66-4431-9e86-0a3a6bb6d846
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 1142-01-25
• Catalog Number: 00-1142-001-25
• Company DUNS: 056038268
• Company Name: Zimmer, Inc.
• Device Count: 5
• 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: 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

Device Dimensions

• Length: 22.9 Centimeter
• Device Size Text, specify: 0
• Length: 22.9 Centimeter
• Device Size Text, specify: 0
• Length: 22.9 Centimeter
• Device Size Text, specify: 0
• Length: 22.9 Centimeter
• Device Size Text, specify: 0
• Length: 22.9 Centimeter
• Device Size Text, specify: 0
• Length: 22.9 Centimeter
• Device Size Text, specify: 0
• Length: 22.9 Centimeter
• Device Size Text, specify: 0
• Length: 22.9 Centimeter
• Device Size Text, specify: 0
• Length: 22.9 Centimeter
• Device Size Text, specify: 0
• Length: 22.9 Centimeter
• Device Size Text, specify: 0
• Length: 22.9 Centimeter
• Device Size Text, specify: 0
• Length: 22.9 Centimeter
• Device Size Text, specify: 0
• Length: 22.9 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00889024024694 [Primary]
GS1	00889024479036 [Unit of Use]

FDA Product Code

• HWE: INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2020-03-23
• Device Publish Date: 2017-01-30

Devices Manufactured by Zimmer, Inc.

• 00889024683884 - G7® Revision Acetabular System: 2026-02-18
• 00889024683938 - G7® Revision Acetabular System: 2026-02-18
• 00889024683945 - G7® Revision Acetabular System: 2026-02-18
• 00889024686496 - G7® Revision Acetabular System: 2026-02-18
• 00889024686502 - G7® Revision Acetabular System: 2026-02-18
• 00889024686519 - G7® Revision Acetabular System: 2026-02-18
• 00889024686526 - G7® Revision Acetabular System: 2026-02-18
• 00889024686533 - G7® Revision Acetabular System: 2026-02-18