6.5mm Cannulated Screw, Half Threaded 060050070

GUDID 06942782411152

Double Medical Technology Inc.

Orthopaedic bone screw, non-bioabsorbable, non-sterile

• Primary Device ID: 06942782411152
• NIH Device Record Key: 87d1f96d-3e56-4398-8199-ce8653ce9709
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 6.5mm Cannulated Screw, Half Threaded
• Version Model Number: 060050070
• Catalog Number: 060050070
• 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: 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 Identifiers

Device Issuing Agency	Device ID
GS1	06942782411152 [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

[06942782411152]

Moist Heat or Steam Sterilization

[06942782411152]

Moist Heat or Steam Sterilization

[06942782411152]

Moist Heat or Steam Sterilization

[06942782411152]

Moist Heat or Steam Sterilization

[06942782411152]

Moist Heat or Steam Sterilization

[06942782411152]

Moist Heat or Steam Sterilization

[06942782411152]

Moist Heat or Steam Sterilization

[06942782411152]

Moist Heat or Steam Sterilization

[06942782411152]

Moist Heat or Steam Sterilization

[06942782411152]

Moist Heat or Steam Sterilization

[06942782411152]

Moist Heat or Steam Sterilization

[06942782411152]

Moist Heat or Steam Sterilization

[06942782411152]

Moist Heat or Steam Sterilization

[06942782411152]

Moist Heat or Steam Sterilization

[06942782411152]

Moist Heat or Steam Sterilization

[06942782411152]

Moist Heat or Steam Sterilization

[06942782411152]

Moist Heat or Steam Sterilization

[06942782411152]

Moist Heat or Steam Sterilization

[06942782411152]

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, Half Threaded]

• 06942782411640: 060050045
• 06942782411237: 060050110
• 06942782411220: 060050105
• 06942782411213: 060050100
• 06942782411206: 060050095
• 06942782411190: 060050090
• 06942782411183: 060050085
• 06942782411176: 060050080
• 06942782411169: 060050075
• 06942782411152: 060050070
• 06942782411145: 060050065
• 06942782411138: 060050060
• 06942782411121: 060050055
• 06942782411114: 060050050