Proximal Aiming Device for Anteroposterior Interlo 110303100

GUDID 06902139111722

Double Medical Technology Inc.

Orthopaedic implant aiming arm

• Primary Device ID: 06902139111722
• NIH Device Record Key: a485f329-01cb-48e1-b4fc-4b4331b25003
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Proximal Aiming Device for Anteroposterior Interlo
• Version Model Number: 110303100
• Catalog Number: 110303100
• Company DUNS: 529366055
• Company Name: Double Medical Technology 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: +865926087101
• Email: info@double-medical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	06902139111722 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K131609

FDA Product Code

• HSB: Rod, Fixation, Intramedullary And Accessories

Sterilization

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

[06902139111722]

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: 2016-09-01

On-Brand Devices [Proximal Aiming Device for Anteroposterior Interlo]

• 06902139111722: 110303100
• 06902139111463: 110300300