Omnia Medical Disc Prep Set 16-6P-NVR1

GUDID 00843511123406

NERVE ROOT RETRACTOR

OMNIA MEDICAL, LLC

Nerve/vessel retractor

• Primary Device ID: 00843511123406
• NIH Device Record Key: 23ace8b0-e13a-4b2a-8c8d-fb7faa1356c5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Omnia Medical Disc Prep Set
• Version Model Number: 16-6P-NVR1
• Catalog Number: 16-6P-NVR1
• Company DUNS: 079467378
• Company Name: OMNIA MEDICAL, LLC
• 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: false
• 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: 3044134851
• Email: customerservice@omniamedical.com
• Phone: 3044134851
• Email: customerservice@omniamedical.com
• Phone: 3044134851
• Email: customerservice@omniamedical.com
• Phone: 3044134851
• Email: customerservice@omniamedical.com
• Phone: 3044134851
• Email: customerservice@omniamedical.com
• Phone: 3044134851
• Email: customerservice@omniamedical.com
• Phone: 3044134851
• Email: customerservice@omniamedical.com
• Phone: 3044134851
• Email: customerservice@omniamedical.com
• Phone: 3044134851
• Email: customerservice@omniamedical.com
• Phone: 3044134851
• Email: customerservice@omniamedical.com
• Phone: 3044134851
• Email: customerservice@omniamedical.com
• Phone: 3044134851
• Email: customerservice@omniamedical.com
• Phone: 3044134851
• Email: customerservice@omniamedical.com
• Phone: 3044134851
• Email: customerservice@omniamedical.com
• Phone: 3044134851
• Email: customerservice@omniamedical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00843511123406 [Primary]

FDA Product Code

• LXH: Orthopedic Manual Surgical Instrument

Sterilization

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

[00843511123406]

Moist Heat or Steam Sterilization

[00843511123406]

Moist Heat or Steam Sterilization

[00843511123406]

Moist Heat or Steam Sterilization

[00843511123406]

Moist Heat or Steam Sterilization

[00843511123406]

Moist Heat or Steam Sterilization

[00843511123406]

Moist Heat or Steam Sterilization

[00843511123406]

Moist Heat or Steam Sterilization

[00843511123406]

Moist Heat or Steam Sterilization

[00843511123406]

Moist Heat or Steam Sterilization

[00843511123406]

Moist Heat or Steam Sterilization

[00843511123406]

Moist Heat or Steam Sterilization

[00843511123406]

Moist Heat or Steam Sterilization

[00843511123406]

Moist Heat or Steam Sterilization

[00843511123406]

Moist Heat or Steam Sterilization

[00843511123406]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-05-17
• Device Publish Date: 2024-05-09

Devices Manufactured by OMNIA MEDICAL, LLC

• 00843511112905 - Omnia Medical Instruments: 2025-02-11 CURETTE, RIGHT RECTANGLE
• 00843511112912 - Omnia Medical Instruments: 2025-02-11 CURETTE, LEFT RECTANGLE
• 00843511112929 - Omnia Medical Instruments: 2025-02-11 CURETTE, CIRCLE
• 00843511112936 - Omnia Medical Instruments: 2025-02-11 CURETTE, ANGLED CIRCLE
• 00843511113148 - TiBrid-SA: 2025-02-11 Extended Tip Awl
• 00843511122164 - Omnia Medical Instruments: 2025-02-11 TS-TO HANDLE
• 00843511128197 - Omnia Medical Disc Prep Instruments: 2025-02-05 Boot Spacer, 12mm
• 00843511128203 - Omnia Medical Disc Prep Instruments: 2025-02-05 Boot Spacer, 14mm