Comprehensive Humeral 120001789

GUDID 00889024685512

Zimmer, Inc.

Instrument tray, reusable

• Primary Device ID: 00889024685512
• NIH Device Record Key: 74783bdf-4236-4bea-a963-d11a83af06b5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Comprehensive Humeral
• Version Model Number: 120001789
• Catalog Number: 120001789
• Company DUNS: 056038268
• Company Name: Zimmer, Inc.
• 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)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00889024685512 [Primary]

FDA Product Code

• FSM: TRAY, SURGICAL, INSTRUMENT

Sterilization

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

[00889024685512]

Moist Heat or Steam Sterilization

[00889024685512]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-09-15
• Device Publish Date: 2025-09-05

On-Brand Devices [Comprehensive Humeral]

• 00889024685512: 120001789
• 00889024685499: 120001785
• 00889024685444: 120001786
• 00889024685420: 120001787
• 00889024685413: 120001788
• 00889024685383: 120001784