"1.5MM" SYSTEM TWIST DRILL 01-7393

GUDID 00841036062750

BIOMET MICROFIXATION, INC

Fluted surgical drill bit, reusable

• Primary Device ID: 00841036062750
• NIH Device Record Key: 74e9b514-822f-4fdb-96cc-e3bfd801e269
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: "1.5MM" SYSTEM TWIST DRILL
• Version Model Number: 01-7393
• Catalog Number: 01-7393
• Company DUNS: 046189866
• Company Name: BIOMET MICROFIXATION, INC
• 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(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841036062750 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K062842

FDA Product Code

• HBE: DRILLS, BURRS, TREPHINES & ACCESSORIES (SIMPLE, POWERED)

Sterilization

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

[00841036062750]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-11-22
• Device Publish Date: 2015-10-11

On-Brand Devices ["1.5MM" SYSTEM TWIST DRILL]

• 00841036062750: 01-7393
• 00841036059897: 01-7392
• 00841036015770: 01-8006
• 00841036014117: 01-7397
• 00841036014100: 01-7395
• 00841036014094: 01-7394
• 00841036013202: 01-7149
• 00841036013189: 01-7146
• 00841036013172: 01-7145
• 00841036013158: 01-7143
• 00841036013127: 01-7140
• 00841036013110: 01-7139
• 00841036012229: 01-6951
• 00841036012212: 01-6950