JuggerStitch™ 110031679

GUDID 00887868245022

Biomet Orthopedics, LLC

Suture trimmer

• Primary Device ID: 00887868245022
• NIH Device Record Key: 039cbecc-a484-461c-afd1-432c00292638
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: JuggerStitch™
• Version Model Number: 110031679
• Catalog Number: 110031679
• Company DUNS: 129278169
• Company Name: Biomet Orthopedics, LLC
• 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: 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	00887868245022 [Primary]

FDA Product Code

• NBH: Accessories, arthroscopic

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: 2019-09-25
• Device Publish Date: 2019-09-17

On-Brand Devices [JuggerStitch™]

• 00880304806832: 110027358
• 00880304806825: 110025571
• 00880304806818: 110025570
• 00880304690073: 110024773
• 00880304690066: 110024772
• 00887868245022: 110031679