LOSPA Knee System, EXULT Knee System

GUDID 08800017204871

Patella Peg Drill

Corentec Co., Ltd

Fluted surgical drill bit, reusable

• Primary Device ID: 08800017204871
• NIH Device Record Key: 31cde672-de91-4815-a4a8-9864e2cdafdf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LOSPA Knee System, EXULT Knee System
• Version Model Number: KZ.020.0007
• Company DUNS: 688739895
• Company Name: Corentec 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: +820269374902
• Email: ra@corentec.com
• Phone: +820269374902
• Email: ra@corentec.com
• Phone: +820269374902
• Email: ra@corentec.com
• Phone: +820269374902
• Email: ra@corentec.com
• Phone: +820269374902
• Email: ra@corentec.com
• Phone: +820269374902
• Email: ra@corentec.com
• Phone: +820269374902
• Email: ra@corentec.com
• Phone: +820269374902
• Email: ra@corentec.com
• Phone: +820269374902
• Email: ra@corentec.com
• Phone: +820269374902
• Email: ra@corentec.com
• Phone: +820269374902
• Email: ra@corentec.com
• Phone: +820269374902
• Email: ra@corentec.com
• Phone: +820269374902
• Email: ra@corentec.com
• Phone: +820269374902
• Email: ra@corentec.com
• Phone: +820269374902
• Email: ra@corentec.com
• Phone: +820269374902
• Email: ra@corentec.com
• Phone: +820269374902
• Email: ra@corentec.com
• Phone: +820269374902
• Email: ra@corentec.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	08800017204871 [Primary]

FDA Product Code

• KIJ: Instrument, Surgical, Orthopedic, Dc-Powered Motor And Accessory/Attachment

Sterilization

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

[08800017204871]

Moist Heat or Steam Sterilization

[08800017204871]

Moist Heat or Steam Sterilization

[08800017204871]

Moist Heat or Steam Sterilization

[08800017204871]

Moist Heat or Steam Sterilization

[08800017204871]

Moist Heat or Steam Sterilization

[08800017204871]

Moist Heat or Steam Sterilization

[08800017204871]

Moist Heat or Steam Sterilization

[08800017204871]

Moist Heat or Steam Sterilization

[08800017204871]

Moist Heat or Steam Sterilization

[08800017204871]

Moist Heat or Steam Sterilization

[08800017204871]

Moist Heat or Steam Sterilization

[08800017204871]

Moist Heat or Steam Sterilization

[08800017204871]

Moist Heat or Steam Sterilization

[08800017204871]

Moist Heat or Steam Sterilization

[08800017204871]

Moist Heat or Steam Sterilization

[08800017204871]

Moist Heat or Steam Sterilization

[08800017204871]

Moist Heat or Steam Sterilization

[08800017204871]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-01-23
• Device Publish Date: 2024-01-15

On-Brand Devices [LOSPA Knee System, EXULT Knee System]

• 08800068981486: Patella Clamp Stylus
• 08800017205267: Patella Clamp Resection Guide Head 2
• 08800017205250: Patella Clamp Resection Guide Head 1
• 08800017204871: Patella Peg Drill