Driver Shaft

GUDID 08806390880855

Jeil Medical Corporation

Surgical screwdriver, reusable

• Primary Device ID: 08806390880855
• NIH Device Record Key: a0a4d2b0-9cfd-4dc9-a87c-bbcaa35a42a7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Driver Shaft
• Version Model Number: 113-HF-623
• Company DUNS: 688811603
• Company Name: Jeil Medical Corporation
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	08806390880855 [Primary]

FDA Product Code

• HXX: Screwdriver

Sterilization

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

[08806390880855]

Moist Heat or Steam Sterilization

[08806390880855]

Moist Heat or Steam Sterilization

[08806390880855]

Moist Heat or Steam Sterilization

[08806390880855]

Moist Heat or Steam Sterilization

[08806390880855]

Moist Heat or Steam Sterilization

[08806390880855]

Moist Heat or Steam Sterilization

[08806390880855]

Moist Heat or Steam Sterilization

[08806390880855]

Moist Heat or Steam Sterilization

[08806390880855]

Moist Heat or Steam Sterilization

[08806390880855]

Moist Heat or Steam Sterilization

[08806390880855]

Moist Heat or Steam Sterilization

[08806390880855]

Moist Heat or Steam Sterilization

[08806390880855]

Moist Heat or Steam Sterilization

[08806390880855]

Moist Heat or Steam Sterilization

[08806390880855]

Moist Heat or Steam Sterilization

[08806390880855]

Moist Heat or Steam Sterilization

[08806390880855]

Moist Heat or Steam Sterilization

[08806390880855]

Moist Heat or Steam Sterilization

[08806390880855]

Moist Heat or Steam Sterilization

[08806390880855]

Moist Heat or Steam Sterilization

[08806390880855]

Moist Heat or Steam Sterilization

[08806390880855]

Moist Heat or Steam Sterilization

[08806390880855]

Moist Heat or Steam Sterilization

[08806390880855]

Moist Heat or Steam Sterilization

[08806390880855]

Moist Heat or Steam Sterilization

[08806390880855]

Moist Heat or Steam Sterilization

[08806390880855]

Moist Heat or Steam Sterilization

[08806390880855]

Moist Heat or Steam Sterilization

[08806390880855]

Moist Heat or Steam Sterilization

[08806390880855]

Moist Heat or Steam Sterilization

[08806390880855]

Moist Heat or Steam Sterilization

[08806390880855]

Moist Heat or Steam Sterilization

[08806390880855]

Moist Heat or Steam Sterilization

[08806390880855]

Moist Heat or Steam Sterilization

[08806390880855]

Moist Heat or Steam Sterilization

[08806390880855]

Moist Heat or Steam Sterilization

[08806390880855]

Moist Heat or Steam Sterilization

[08806390880855]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-10-27
• Device Publish Date: 2020-10-19

Devices Manufactured by Jeil Medical Corporation

• 08800089479832 - Surgical Instrument: 2026-02-05
• 08800089479849 - Surgical Instrument: 2026-02-05
• 08800089479856 - Surgical Instrument: 2026-02-05
• 08800089479863 - Surgical Instrument: 2026-02-05
• 08800089479429 - Surgical Instrument: 2026-01-14
• 08800089479436 - Surgical Instrument: 2026-01-14
• 08800089479443 - ARIX System Bone Screw: 2026-01-14
• 08800089454549 - ARIX Femur Nail System: 2026-01-06