7.3mm Cannulated Screw, Long Threaded 060070055

GUDID 06942782409098

Double Medical Technology Inc.

Orthopaedic bone screw, non-bioabsorbable, non-sterile

• Primary Device ID: 06942782409098
• NIH Device Record Key: 92c25c0f-550c-4aab-a32f-98f0fa22ad9e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 7.3mm Cannulated Screw, Long Threaded
• Version Model Number: 060070055
• Catalog Number: 060070055
• 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: 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 Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	06942782409098 [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

[06942782409098]

Moist Heat or Steam Sterilization

[06942782409098]

Moist Heat or Steam Sterilization

[06942782409098]

Moist Heat or Steam Sterilization

[06942782409098]

Moist Heat or Steam Sterilization

[06942782409098]

Moist Heat or Steam Sterilization

[06942782409098]

Moist Heat or Steam Sterilization

[06942782409098]

Moist Heat or Steam Sterilization

[06942782409098]

Moist Heat or Steam Sterilization

[06942782409098]

Moist Heat or Steam Sterilization

[06942782409098]

Moist Heat or Steam Sterilization

[06942782409098]

Moist Heat or Steam Sterilization

[06942782409098]

Moist Heat or Steam Sterilization

[06942782409098]

Moist Heat or Steam Sterilization

[06942782409098]

Moist Heat or Steam Sterilization

[06942782409098]

Moist Heat or Steam Sterilization

[06942782409098]

Moist Heat or Steam Sterilization

[06942782409098]

Moist Heat or Steam Sterilization

[06942782409098]

Moist Heat or Steam Sterilization

[06942782409098]

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, Long Threaded]

• 06942782409203: 060070110
• 06942782409197: 060070105
• 06942782409180: 060070100
• 06942782409173: 060070095
• 06942782409166: 060070090
• 06942782409159: 060070085
• 06942782409142: 060070080
• 06942782409135: 060070075
• 06942782409128: 060070070
• 06942782409111: 060070065
• 06942782409104: 060070060
• 06942782409098: 060070055
• 06942782409081: 060070050