GPS® III 800-0745

GUDID 00880304460652

Biomet Biologics, LLC

Haematological concentrate system

• Primary Device ID: 00880304460652
• NIH Device Record Key: 06d8bb70-3cf0-4c8b-8835-29760d84a770
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: GPS® III
• Version Model Number: 800-0745
• Catalog Number: 800-0745
• Company DUNS: 802003074
• Company Name: Biomet Biologics, LLC
• 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)348-9500
• Email: customerservice@zimmerbiomet.com

Device Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00880304460652 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• BK070026

FDA Product Code

• KSS: SUPPLIES, BLOOD-BANK

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-02-05
• Device Publish Date: 2016-11-03

On-Brand Devices [GPS® III]

• 00880304460652: 800-0745
• 00880304460645: 800-0744