2.0/2.4MM FRACTURE SYSTEM 24-1194

GUDID 00841036036256

2.4MM X-LOCK CROSS-DRIVE SHORT BLADE

BIOMET MICROFIXATION, INC

Surgical screwdriver, reusable

• Primary Device ID: 00841036036256
• NIH Device Record Key: 4de80be7-6976-4057-8e92-ac86556e39cc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 2.0/2.4MM FRACTURE SYSTEM
• Version Model Number: 24-1194
• Catalog Number: 24-1194
• Company DUNS: 046189866
• Company Name: BIOMET MICROFIXATION, INC
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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: 904-741-4400
• Email: FXJAX-ORDERS@BIOMET.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841036036256 [Primary]

FDA Product Code

• HXX: Screwdriver

Sterilization

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

[00841036036256]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-10-05
• Device Publish Date: 2014-09-17

On-Brand Devices [2.0/2.4MM FRACTURE SYSTEM]

• 00841036036225: 24-1186
• 00841036070373: 24-1082
• 00841036036256: 2.4MM X-LOCK CROSS-DRIVE SHORT BLADE
• 00841036036072: PLATE HOLDING FORCEPS
• 00841036036027: 24-1080
• 00841036036010: 24-1068
• 00841036036003: 24-1066
• 00841036035990: 24-1064
• 00841036035983: 24-1060
• 00841036035969: 24-1056
• 00841036035952: 24-1054
• 00841036035945: 24-1052
• 00841036035938: 24-1050