COMPREHENSIVE® 31-406182

GUDID 00880304456372

Biomet Orthopedics, LLC

Fluted surgical drill bit, reusable

• Primary Device ID: 00880304456372
• NIH Device Record Key: 0c1ab619-d0d3-4dd2-bdb5-1fe7369d4420
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: COMPREHENSIVE®
• Version Model Number: 31-406182
• Catalog Number: 31-406182
• 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 Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00880304456372 [Primary]

FDA Product Code

• HTW: BIT, DRILL

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-11-22
• Device Publish Date: 2017-07-28

On-Brand Devices [COMPREHENSIVE®]

• 00880304466616: 595272
• 00880304461826: 595260
• 00880304461796: 595257
• 00880304461116: 595258
• 00880304456969: 595264
• 00880304456594: 31-111115
• 00880304456563: 31-111116
• 00880304456556: 31-406636
• 00880304456372: 31-406182
• 00887868505065: 406183
• 00887868525674: XRAY000164
• 00887868578250: XRAY000164