JuggerStitch™ 110027358

GUDID 00880304806832

Biomet Orthopedics, LLC

Arthroscopic access cannula, single-use

• Primary Device ID: 00880304806832
• NIH Device Record Key: 818428c4-a777-48c7-8c89-9d3ecf8946c1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: JuggerStitch™
• Version Model Number: 110027358
• Catalog Number: 110027358
• Company DUNS: 129278169
• Company Name: Biomet Orthopedics, 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	00880304806832 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K150424

FDA Product Code

• MBI: Fastener, fixation, nondegradable, soft tissue

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: 2019-09-18
• Device Publish Date: 2017-03-16

On-Brand Devices [JuggerStitch™]

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