5.0mm Dual Core Locking Screw 071260080

GUDID 06942782417338

Double Medical Technology Inc.

Tibia nail, non-sterile

• Primary Device ID: 06942782417338
• NIH Device Record Key: a310c04e-9e0e-46da-a949-2f708fec3ab8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 5.0mm Dual Core Locking Screw
• Version Model Number: 071260080
• Catalog Number: 071260080
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• 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 Dimensions

• Device Size Text, specify: 0
• Length: 80 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	06942782417338 [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

[06942782417338]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-01

On-Brand Devices [5.0mm Dual Core Locking Screw]

• 06942782417338: 071260080
• 06942782417321: 071260075
• 06942782417314: 071260070
• 06942782417307: 071260065
• 06942782417291: 071260060
• 06942782417284: 071260055
• 06942782417277: 071260050
• 06942782417260: 071260045
• 06942782417253: 071260040
• 06942782417246: 071260035
• 06942782417239: 071260030