"2.0/2.4MM" FRACTURE SYSTEM 24-1126

GUDID 00841036036119

BIOMET MICROFIXATION, INC

Surgical drill guide, reusable

• Primary Device ID: 00841036036119
• NIH Device Record Key: 5b02a0e1-1285-4d29-8fc8-7c04291b703d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: "2.0/2.4MM" FRACTURE SYSTEM
• Version Model Number: 24-1126
• Catalog Number: 24-1126
• 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: false
• 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	00841036036119 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K121589

FDA Product Code

• JEY: PLATE, BONE

Sterilization

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

[00841036036119]

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 ["2.0/2.4MM" FRACTURE SYSTEM]

• 00841036036218: 24-1154
• 00841036036126: 24-1128
• 00841036036119: 24-1126
• 00841036036171: 24-1144
• 00841036036102: 24-1124
• 00841036036089: 24-1112
• 00841036018443: 01-9728