3.0mm Heberden Screw 060010034

GUDID 06942782411930

Double Medical Technology Inc.

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

• Primary Device ID: 06942782411930
• NIH Device Record Key: 20cfd4de-3287-49fe-9d5c-581d79f30086
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 3.0mm Heberden Screw
• Version Model Number: 060010034
• Catalog Number: 060010034
• 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: 34 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 34 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 34 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 34 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 34 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 34 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 34 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 34 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 34 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 34 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 34 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 34 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 34 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 34 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 34 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 34 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 34 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 34 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 34 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	06942782411930 [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

[06942782411930]

Moist Heat or Steam Sterilization

[06942782411930]

Moist Heat or Steam Sterilization

[06942782411930]

Moist Heat or Steam Sterilization

[06942782411930]

Moist Heat or Steam Sterilization

[06942782411930]

Moist Heat or Steam Sterilization

[06942782411930]

Moist Heat or Steam Sterilization

[06942782411930]

Moist Heat or Steam Sterilization

[06942782411930]

Moist Heat or Steam Sterilization

[06942782411930]

Moist Heat or Steam Sterilization

[06942782411930]

Moist Heat or Steam Sterilization

[06942782411930]

Moist Heat or Steam Sterilization

[06942782411930]

Moist Heat or Steam Sterilization

[06942782411930]

Moist Heat or Steam Sterilization

[06942782411930]

Moist Heat or Steam Sterilization

[06942782411930]

Moist Heat or Steam Sterilization

[06942782411930]

Moist Heat or Steam Sterilization

[06942782411930]

Moist Heat or Steam Sterilization

[06942782411930]

Moist Heat or Steam Sterilization

[06942782411930]

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 [3.0mm Heberden Screw]

• 06942782439354: 060010018
• 06942782411961: 060010040
• 06942782411954: 060010038
• 06942782411947: 060010036
• 06942782411930: 060010034
• 06942782410452: 060010032
• 06942782410094: 060010030
• 06942782410087: 060010028
• 06942782409395: 060010026
• 06942782409388: 060010024
• 06942782409371: 060010022
• 06942782409364: 060010020
• 06942782409340: 060010016
• 06942782409333: 060010014