POWER HEX SCREW DRIVER, SHORT 5.0mm 0491-100

GUDID 00848665014228

ADVANCED ORTHOPEDIC SOLUTIONS INC

Surgical screwdriver, reusable

• Primary Device ID: 00848665014228
• NIH Device Record Key: 36a23962-cd2b-4a94-9944-9d3563955205
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: POWER HEX SCREW DRIVER, SHORT 5.0mm
• Version Model Number: 0491-100
• Catalog Number: 0491-100
• Company DUNS: 117858154
• Company Name: ADVANCED ORTHOPEDIC SOLUTIONS INC
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• 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: 310-533-9966
• Email: regaffairs@aosortho.com
• Phone: 310-533-9966
• Email: regaffairs@aosortho.com
• Phone: 310-533-9966
• Email: regaffairs@aosortho.com
• Phone: 310-533-9966
• Email: regaffairs@aosortho.com
• Phone: 310-533-9966
• Email: regaffairs@aosortho.com
• Phone: 310-533-9966
• Email: regaffairs@aosortho.com
• Phone: 310-533-9966
• Email: regaffairs@aosortho.com
• Phone: 310-533-9966
• Email: regaffairs@aosortho.com
• Phone: 310-533-9966
• Email: regaffairs@aosortho.com
• Phone: 310-533-9966
• Email: regaffairs@aosortho.com
• Phone: 310-533-9966
• Email: regaffairs@aosortho.com
• Phone: 310-533-9966
• Email: regaffairs@aosortho.com
• Phone: 310-533-9966
• Email: regaffairs@aosortho.com
• Phone: 310-533-9966
• Email: regaffairs@aosortho.com
• Phone: 310-533-9966
• Email: regaffairs@aosortho.com
• Phone: 310-533-9966
• Email: regaffairs@aosortho.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00848665014228 [Primary]

FDA Product Code

• LXH: Orthopedic Manual Surgical Instrument

Sterilization

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

[00848665014228]

Moist Heat or Steam Sterilization

[00848665014228]

Moist Heat or Steam Sterilization

[00848665014228]

Moist Heat or Steam Sterilization

[00848665014228]

Moist Heat or Steam Sterilization

[00848665014228]

Moist Heat or Steam Sterilization

[00848665014228]

Moist Heat or Steam Sterilization

[00848665014228]

Moist Heat or Steam Sterilization

[00848665014228]

Moist Heat or Steam Sterilization

[00848665014228]

Moist Heat or Steam Sterilization

[00848665014228]

Moist Heat or Steam Sterilization

[00848665014228]

Moist Heat or Steam Sterilization

[00848665014228]

Moist Heat or Steam Sterilization

[00848665014228]

Moist Heat or Steam Sterilization

[00848665014228]

Moist Heat or Steam Sterilization

[00848665014228]

Moist Heat or Steam Sterilization

[00848665014228]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2020-01-27
• Device Publish Date: 2016-02-24

Devices Manufactured by ADVANCED ORTHOPEDIC SOLUTIONS INC

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• 00848665000658 - AOS Drill, AO Style, 2.9mm x 100mm: 2020-06-08
• 00848665001235 - AOS CANCELLOUS TAP 3.5mm: 2020-06-08
• 00848665027624 - SUPRAPATELLAR TIBIAL ENTRY SHEATH: 2020-06-08
• 00848665028041 - T10 Screwdriver, Short: 2020-06-08
• 00848665028096 - 3.5mm Calibrated Drill: 2020-06-08
• 00848665028119 - AOS 2.6mm Solid Reamer: 2020-06-08
• 00848665028782 - T10 Screwdriver, Solid: 2020-06-08