6.5mm Cannulated Screw, Fully Threaded 060060055

GUDID 06942782411251

Double Medical Technology Inc.

Orthopaedic bone screw, non-bioabsorbable, non-sterile

• Primary Device ID: 06942782411251
• NIH Device Record Key: 7396a2ff-1bbf-4768-a2e2-7563e57f4763
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 6.5mm Cannulated Screw, Fully Threaded
• Version Model Number: 060060055
• Catalog Number: 060060055
• 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

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 55 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 55 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 55 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 55 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 55 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 55 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 55 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 55 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 55 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 55 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 55 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 55 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 55 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 55 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 55 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 55 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 55 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 55 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 55 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	06942782411251 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K130108

FDA Product Code

• HRS: Plate, Fixation, Bone

Sterilization

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

[06942782411251]

Moist Heat or Steam Sterilization

[06942782411251]

Moist Heat or Steam Sterilization

[06942782411251]

Moist Heat or Steam Sterilization

[06942782411251]

Moist Heat or Steam Sterilization

[06942782411251]

Moist Heat or Steam Sterilization

[06942782411251]

Moist Heat or Steam Sterilization

[06942782411251]

Moist Heat or Steam Sterilization

[06942782411251]

Moist Heat or Steam Sterilization

[06942782411251]

Moist Heat or Steam Sterilization

[06942782411251]

Moist Heat or Steam Sterilization

[06942782411251]

Moist Heat or Steam Sterilization

[06942782411251]

Moist Heat or Steam Sterilization

[06942782411251]

Moist Heat or Steam Sterilization

[06942782411251]

Moist Heat or Steam Sterilization

[06942782411251]

Moist Heat or Steam Sterilization

[06942782411251]

Moist Heat or Steam Sterilization

[06942782411251]

Moist Heat or Steam Sterilization

[06942782411251]

Moist Heat or Steam Sterilization

[06942782411251]

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 [6.5mm Cannulated Screw, Fully Threaded]

• 06942782411626: 060060045
• 06942782411619: 060060040
• 06942782411367: 060060110
• 06942782411350: 060060105
• 06942782411343: 060060100
• 06942782411336: 060060095
• 06942782411329: 060060090
• 06942782411312: 060060085
• 06942782411305: 060060080
• 06942782411299: 060060075
• 06942782411282: 060060070
• 06942782411275: 060060065
• 06942782411268: 060060060
• 06942782411251: 060060055
• 06942782411244: 060060050