Biomet® 800-0270

GUDID 00880304484757

Biomet Biologics, LLC

Open-surgery adhesive/sealant applicator, dual-channel

• Primary Device ID: 00880304484757
• NIH Device Record Key: b999edf1-6d56-4413-8fb9-bb21355b5c53
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Biomet®
• Version Model Number: 800-0270
• Catalog Number: 800-0270
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	00880304484757 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K091722

FDA Product Code

• FMF: Syringe, piston

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: 2019-06-19
• Device Publish Date: 2019-06-11

On-Brand Devices [Biomet®]

• 00880304484757: 800-0270
• 00880304430495: 800-0505
• 00880304400085: 800-0508