HKT Anatomical Lciking Trauma System 16214-11015

GUDID 08809596478550

Torque Driver 1.5Nm

Hankil Tech Medical Co., Ltd.

Surgical instrument handle, torque-limiting

• Primary Device ID: 08809596478550
• NIH Device Record Key: 7fedf24d-63f6-4e9b-befb-d7bb74339e75
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HKT Anatomical Lciking Trauma System
• Version Model Number: 16214-11015
• Catalog Number: 16214-11015
• Company DUNS: 688499031
• Company Name: Hankil Tech Medical Co., Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• 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: +821090544233
• Email: yh_park@ostymeditech.com
• Phone: +821090544233
• Email: yh_park@ostymeditech.com
• Phone: +821090544233
• Email: yh_park@ostymeditech.com
• Phone: +821090544233
• Email: yh_park@ostymeditech.com
• Phone: +821090544233
• Email: yh_park@ostymeditech.com
• Phone: +821090544233
• Email: yh_park@ostymeditech.com
• Phone: +821090544233
• Email: yh_park@ostymeditech.com
• Phone: +821090544233
• Email: yh_park@ostymeditech.com
• Phone: +821090544233
• Email: yh_park@ostymeditech.com
• Phone: +821090544233
• Email: yh_park@ostymeditech.com
• Phone: +821090544233
• Email: yh_park@ostymeditech.com
• Phone: +821090544233
• Email: yh_park@ostymeditech.com
• Phone: +821090544233
• Email: yh_park@ostymeditech.com
• Phone: +821090544233
• Email: yh_park@ostymeditech.com
• Phone: +821090544233
• Email: yh_park@ostymeditech.com
• Phone: +821090544233
• Email: yh_park@ostymeditech.com
• Phone: +821090544233
• Email: yh_park@ostymeditech.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	08809596478550 [Primary]

FDA Product Code

• HXX: Screwdriver

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[08809596478550]

Moist Heat or Steam Sterilization

[08809596478550]

Moist Heat or Steam Sterilization

[08809596478550]

Moist Heat or Steam Sterilization

[08809596478550]

Moist Heat or Steam Sterilization

[08809596478550]

Moist Heat or Steam Sterilization

[08809596478550]

Moist Heat or Steam Sterilization

[08809596478550]

Moist Heat or Steam Sterilization

[08809596478550]

Moist Heat or Steam Sterilization

[08809596478550]

Moist Heat or Steam Sterilization

[08809596478550]

Moist Heat or Steam Sterilization

[08809596478550]

Moist Heat or Steam Sterilization

[08809596478550]

Moist Heat or Steam Sterilization

[08809596478550]

Moist Heat or Steam Sterilization

[08809596478550]

Moist Heat or Steam Sterilization

[08809596478550]

Moist Heat or Steam Sterilization

[08809596478550]

Moist Heat or Steam Sterilization

[08809596478550]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-08-21
• Device Publish Date: 2024-08-13

On-Brand Devices [HKT Anatomical Lciking Trauma System]

• 08809946780432: Bender 180mm
• 08809946780418: 3.0mm Variable Drill Guide (w/o Grip)
• 08809596478550: Torque Driver 1.5Nm
• 08809596477935: 2.5Hex/210mm Screw Driver
• 8809596471902: 12203-35034
• 8809596471889: 12203-35030
• 08809407600699: 11424-92050
• 08809407600644: 11424-92040
• 08809407600606: 11424-92035
• 08809407600590: 11424-92020