4.0mm Cannulated Screw 060020070

GUDID 06942782472528

Double Medical Technology Inc.

Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile

• Primary Device ID: 06942782472528
• NIH Device Record Key: 93060188-2b19-4de0-9688-01fdde2fefc8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 4.0mm Cannulated Screw
• Version Model Number: 060020070
• Catalog Number: 060020070
• 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: 70 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 70 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 70 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 70 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 70 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 70 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 70 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 70 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 70 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 70 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 70 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 70 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 70 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 70 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 70 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 70 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 70 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 70 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 70 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	06942782472528 [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

[06942782472528]

Moist Heat or Steam Sterilization

[06942782472528]

Moist Heat or Steam Sterilization

[06942782472528]

Moist Heat or Steam Sterilization

[06942782472528]

Moist Heat or Steam Sterilization

[06942782472528]

Moist Heat or Steam Sterilization

[06942782472528]

Moist Heat or Steam Sterilization

[06942782472528]

Moist Heat or Steam Sterilization

[06942782472528]

Moist Heat or Steam Sterilization

[06942782472528]

Moist Heat or Steam Sterilization

[06942782472528]

Moist Heat or Steam Sterilization

[06942782472528]

Moist Heat or Steam Sterilization

[06942782472528]

Moist Heat or Steam Sterilization

[06942782472528]

Moist Heat or Steam Sterilization

[06942782472528]

Moist Heat or Steam Sterilization

[06942782472528]

Moist Heat or Steam Sterilization

[06942782472528]

Moist Heat or Steam Sterilization

[06942782472528]

Moist Heat or Steam Sterilization

[06942782472528]

Moist Heat or Steam Sterilization

[06942782472528]

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 [4.0mm Cannulated Screw]

• 06942782472535: 060020075
• 06942782472528: 060020070
• 06942782472511: 060020065
• 06942782409319: 060020060
• 06942782409302: 060020055
• 06942782409296: 060020050
• 06942782409289: 060020045
• 06942782409272: 060020040
• 06942782409265: 060020035
• 06942782409258: 060020030
• 06942782409241: 060020028
• 06942782409234: 060020026