2.0MM LOCKING FRACTURE SYSTEM 20-4544T

GUDID 00841036132026

BIOMET MICROFIXATION, INC

Surgical implant template, reusable

• Primary Device ID: 00841036132026
• NIH Device Record Key: c662d291-f625-426e-a0e0-f2dc8c3f9ade
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 2.0MM LOCKING FRACTURE SYSTEM
• Version Model Number: 20-4544T
• Catalog Number: 20-4544T
• 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: 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	00841036132026 [Primary]

FDA Product Code

• HWT: TEMPLATE

Sterilization

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

[00841036132026]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-09-28
• Device Publish Date: 2018-08-28

On-Brand Devices [2.0MM LOCKING FRACTURE SYSTEM]

• 00841036199623: SP-1710
• 00841036132026: 20-4544T
• 00841036073855: 20-4544
• 00841036073206: 20-4540T
• 00841036072797: 20-4504T
• 00841036069414: 20-4504
• 00841036067281: 20-4541
• 00841036066505: 20-4540
• 00841036066215: 20-4516T
• 00841036066208: 20-4506T
• 00841036065911: 20-4507T
• 00841036060459: 20-4516
• 00841036060435: 20-4506
• 00841036059576: 20-4507