Freehand Drill Guide MDS110807

GUDID 10812269020456

Freehand Drill Guide

MIAMI DEVICE SOLUTIONS LLC

Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile

• Primary Device ID: 10812269020456
• NIH Device Record Key: 48bacc05-4df3-462c-8d79-cfc90aa63aa4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Freehand Drill Guide
• Version Model Number: MDS110807
• Catalog Number: MDS110807
• Company DUNS: 078703080
• Company Name: MIAMI DEVICE SOLUTIONS 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: 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: (786) 422-1400
• Email: customerservice@miamidevicesolutions.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	10812269020456 [Primary]

FDA Product Code

• HWC: Screw, Fixation, Bone

Sterilization

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

[10812269020456]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-04-06
• Device Publish Date: 2017-01-25

On-Brand Devices [Freehand Drill Guide]

• 10812269025567: Freehand Drill Guide, 2.0T
• 10812269025536: Freehand Drill Guide, Short, 2.7T
• 10812269020456: Freehand Drill Guide