2.0S-LCP Adaption Plate 021030006

GUDID 06942782477059

Double Medical Technology Inc.

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

• Primary Device ID: 06942782477059
• NIH Device Record Key: 68a8afe4-f57e-4f7d-ba40-1719fc0af344
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 2.0S-LCP Adaption Plate
• Version Model Number: 021030006
• Catalog Number: 021030006
• 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

Device Dimensions

• Length: 40.6 Millimeter
• Width: 5 Millimeter
• Device Size Text, specify: 0
• Length: 40.6 Millimeter
• Width: 5 Millimeter
• Device Size Text, specify: 0
• Length: 40.6 Millimeter
• Width: 5 Millimeter
• Device Size Text, specify: 0
• Length: 40.6 Millimeter
• Width: 5 Millimeter
• Device Size Text, specify: 0
• Length: 40.6 Millimeter
• Width: 5 Millimeter
• Device Size Text, specify: 0
• Length: 40.6 Millimeter
• Width: 5 Millimeter
• Device Size Text, specify: 0
• Length: 40.6 Millimeter
• Width: 5 Millimeter
• Device Size Text, specify: 0
• Length: 40.6 Millimeter
• Width: 5 Millimeter
• Device Size Text, specify: 0
• Length: 40.6 Millimeter
• Width: 5 Millimeter
• Device Size Text, specify: 0
• Length: 40.6 Millimeter
• Width: 5 Millimeter
• Device Size Text, specify: 0
• Length: 40.6 Millimeter
• Width: 5 Millimeter
• Device Size Text, specify: 0
• Length: 40.6 Millimeter
• Width: 5 Millimeter
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	06942782477059 [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

[06942782477059]

Moist Heat or Steam Sterilization

[06942782477059]

Moist Heat or Steam Sterilization

[06942782477059]

Moist Heat or Steam Sterilization

[06942782477059]

Moist Heat or Steam Sterilization

[06942782477059]

Moist Heat or Steam Sterilization

[06942782477059]

Moist Heat or Steam Sterilization

[06942782477059]

Moist Heat or Steam Sterilization

[06942782477059]

Moist Heat or Steam Sterilization

[06942782477059]

Moist Heat or Steam Sterilization

[06942782477059]

Moist Heat or Steam Sterilization

[06942782477059]

Moist Heat or Steam Sterilization

[06942782477059]

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 [2.0S-LCP Adaption Plate]

• 06942782477059: 021030006
• 06942782454227: 021030012