BENCOX THR Instruments System

GUDID 08800017270517

Reamer 63mm

Corentec Co., Ltd

Bone-resection orthopaedic reamer, reusable Bone-resection orthopaedic reamer, reusable Bone-resection orthopaedic reamer, reusable Bone-resection orthopaedic reamer, reusable Bone-resection orthopaedic reamer, reusable Bone-resection orthopaedic reamer, reusable Bone-resection orthopaedic reamer, reusable Bone-resection orthopaedic reamer, reusable Bone-resection orthopaedic reamer, reusable Bone-resection orthopaedic reamer, reusable Bone-resection orthopaedic reamer, reusable Bone-resection orthopaedic reamer, reusable Bone-resection orthopaedic reamer, reusable

• Primary Device ID: 08800017270517
• NIH Device Record Key: 963437ff-ce24-4ec8-8154-cd1710acf59d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BENCOX THR Instruments System
• Version Model Number: HA.091.0063
• 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: +82269374902
• Email: ra@corentec.com
• Phone: +82269374902
• Email: ra@corentec.com
• Phone: +82269374902
• Email: ra@corentec.com
• Phone: +82269374902
• Email: ra@corentec.com
• Phone: +82269374902
• Email: ra@corentec.com
• Phone: +82269374902
• Email: ra@corentec.com
• Phone: +82269374902
• Email: ra@corentec.com
• Phone: +82269374902
• Email: ra@corentec.com
• Phone: +82269374902
• Email: ra@corentec.com
• Phone: +82269374902
• Email: ra@corentec.com
• Phone: +82269374902
• Email: ra@corentec.com
• Phone: +82269374902
• Email: ra@corentec.com
• Phone: +82269374902
• Email: ra@corentec.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	08800017270517 [Primary]

FDA Product Code

• HWE: Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment

Sterilization

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

[08800017270517]

Moist Heat or Steam Sterilization

[08800017270517]

Moist Heat or Steam Sterilization

[08800017270517]

Moist Heat or Steam Sterilization

[08800017270517]

Moist Heat or Steam Sterilization

[08800017270517]

Moist Heat or Steam Sterilization

[08800017270517]

Moist Heat or Steam Sterilization

[08800017270517]

Moist Heat or Steam Sterilization

[08800017270517]

Moist Heat or Steam Sterilization

[08800017270517]

Moist Heat or Steam Sterilization

[08800017270517]

Moist Heat or Steam Sterilization

[08800017270517]

Moist Heat or Steam Sterilization

[08800017270517]

Moist Heat or Steam Sterilization

[08800017270517]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-02-27
• Device Publish Date: 2024-02-19

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• 08800017276489 - Lospa Modular Knee System: 2024-04-03 Tibial Keel Punch (L)
• 08800017278247 - Lospa Modular Knee System: 2024-04-03 Locking Rod Impactor
• 08806373895111 - Lospa Knee System Instrument: 2024-03-25 Patella Cailpers
• 08809945890774 - Exult Knee Replacement System Instrument: 2024-03-25 Patella Peg Drill
• 08800017270357 - BENCOX THR Instruments Hip System: 2024-02-27 Reamer 47mm