ULTRA-DRIVE® 423834

GUDID 00880304372924

Biomet Orthopedics, LLC

Surgical power tool irrigation-control device

• Primary Device ID: 00880304372924
• NIH Device Record Key: 04b645ba-1595-41a1-9a57-ab72b846646c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ULTRA-DRIVE®
• Version Model Number: 423834
• Catalog Number: 423834
• 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	00880304372924 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K031280

FDA Product Code

• JXE: DEVICE, NERVE CONDUCTION VELOCITY MEASUREMENT

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: 2018-11-22
• Device Publish Date: 2016-09-25

On-Brand Devices [ULTRA-DRIVE®]

• 00880304372924: 423834
• 00880304372917: 423833
• 00887868523731: 423874