7.3mm Cannulated Screw, Short Threaded 060080110

GUDID 06942782409074

Double Medical Technology Inc.

Orthopaedic bone screw, non-bioabsorbable, non-sterile

• Primary Device ID: 06942782409074
• NIH Device Record Key: 45072a9b-763e-4671-8558-05e2564c9bc2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 7.3mm Cannulated Screw, Short Threaded
• Version Model Number: 060080110
• Catalog Number: 060080110
• 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
• Phone: +865926087101
• Email: info@double-medical.com
• Phone: +865926087101
• Email: info@double-medical.com
• Phone: +865926087101
• Email: info@double-medical.com
• Phone: +865926087101
• Email: info@double-medical.com
• Phone: +865926087101
• Email: info@double-medical.com
• Phone: +865926087101
• Email: info@double-medical.com
• Phone: +865926087101
• Email: info@double-medical.com
• Phone: +865926087101
• Email: info@double-medical.com
• Phone: +865926087101
• Email: info@double-medical.com
• Phone: +865926087101
• Email: info@double-medical.com
• Phone: +865926087101
• Email: info@double-medical.com
• Phone: +865926087101
• Email: info@double-medical.com
• Phone: +865926087101
• Email: info@double-medical.com
• Phone: +865926087101
• Email: info@double-medical.com
• Phone: +865926087101
• Email: info@double-medical.com
• Phone: +865926087101
• Email: info@double-medical.com
• Phone: +865926087101
• Email: info@double-medical.com
• Phone: +865926087101
• Email: info@double-medical.com

Device Dimensions

• Length: 110 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 110 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 110 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 110 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 110 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 110 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 110 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 110 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 110 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 110 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 110 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 110 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 110 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 110 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 110 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 110 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 110 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 110 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 110 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	06942782409074 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K130108

FDA Product Code

• HWC: Screw, Fixation, Bone

Sterilization

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

[06942782409074]

Moist Heat or Steam Sterilization

[06942782409074]

Moist Heat or Steam Sterilization

[06942782409074]

Moist Heat or Steam Sterilization

[06942782409074]

Moist Heat or Steam Sterilization

[06942782409074]

Moist Heat or Steam Sterilization

[06942782409074]

Moist Heat or Steam Sterilization

[06942782409074]

Moist Heat or Steam Sterilization

[06942782409074]

Moist Heat or Steam Sterilization

[06942782409074]

Moist Heat or Steam Sterilization

[06942782409074]

Moist Heat or Steam Sterilization

[06942782409074]

Moist Heat or Steam Sterilization

[06942782409074]

Moist Heat or Steam Sterilization

[06942782409074]

Moist Heat or Steam Sterilization

[06942782409074]

Moist Heat or Steam Sterilization

[06942782409074]

Moist Heat or Steam Sterilization

[06942782409074]

Moist Heat or Steam Sterilization

[06942782409074]

Moist Heat or Steam Sterilization

[06942782409074]

Moist Heat or Steam Sterilization

[06942782409074]

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 [7.3mm Cannulated Screw, Short Threaded]

• 06942782409074: 060080110
• 06942782409067: 060080105
• 06942782409050: 060080100
• 06942782409043: 060080095
• 06942782409036: 060080090
• 06942782409029: 060080085
• 06942782409012: 060080080
• 06942782409005: 060080075
• 06942782408992: 060080070
• 06942782408985: 060080065
• 06942782408978: 060080060
• 06942782408961: 060080055
• 06942782408954: 060080050