Polyaxial Drill Guide Tube MDS110801

GUDID 10812269020401

Polyaxial Drill Guide Tube

MIAMI DEVICE SOLUTIONS LLC

Surgical drill guide, reusable

• Primary Device ID: 10812269020401
• NIH Device Record Key: eb3928a8-d04d-4fd1-b7e2-86a4ed71e1d6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Polyaxial Drill Guide Tube
• Version Model Number: MDS110801
• Catalog Number: MDS110801
• 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	10812269020401 [Primary]

FDA Product Code

• HWC: Screw, Fixation, Bone

Sterilization

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

[10812269020401]

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 [Polyaxial Drill Guide Tube]

• 10812269024997: Polyaxial Drill Guide Tube, 2.0T
• 10812269020401: Polyaxial Drill Guide Tube