CANNULATED DRILL BIT AO 110027744

GUDID 00887868138522

Biomet Orthopedics, LLC

Fluted surgical drill bit, single-use, non-sterile

• Primary Device ID: 00887868138522
• NIH Device Record Key: 38e57064-f79a-464a-8ab5-2d54ef7728c9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CANNULATED DRILL BIT AO
• Version Model Number: 110027744
• Catalog Number: 110027744
• 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: false
• 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	00887868138522 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K142658

FDA Product Code

• HWC: Screw, fixation, bone

Sterilization

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

[00887868138522]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-01-21
• Device Publish Date: 2018-12-19

On-Brand Devices [CANNULATED DRILL BIT AO]

• 00887868138522: 110027744
• 00887868137891: 110018532
• 00887868137860: 110027745
• 00887868467219: 110018532
• 00887868469954: 110027745