Zimmer Biomet® 12/14 Spherical Head Trials 110048033

GUDID 00887868585661

Zimmer, Inc.

Device sterilization/disinfection container, reusable

• Primary Device ID: 00887868585661
• NIH Device Record Key: 6a1ce1c2-2eab-4472-80d4-b3dfb9152e30
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Zimmer Biomet® 12/14 Spherical Head Trials
• Version Model Number: 110048033
• Catalog Number: 110048033
• 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 Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887868585661 [Primary]

FDA Product Code

• FSM: TRAY, SURGICAL, INSTRUMENT

Sterilization

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

[00887868585661]

Moist Heat or Steam Sterilization

[00887868585661]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-11-19
• Device Publish Date: 2024-11-11

On-Brand Devices [Zimmer Biomet® 12/14 Spherical Head Trials]

• 00887868585654: 110040312
• 00887868585661: 110048033