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

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• 00843511128173 - Omnia Medical Golden Spike: 2024-11-29 Golden Spike Driver, not threaded
• 00843511111823 - Omnia Medical TiBrid™-SA: 2024-06-20 TiBrid™-SA PLATE, 30mm, L1-L5
• 00843511111830 - Omnia Medical TiBrid™-SA: 2024-06-20 TiBrid™-SA PLATE, 32mm, L1-L5
• 00843511111847 - Omnia Medical TiBrid™-SA: 2024-06-20 TiBrid™-SA PLATE, 34mm, L1-L5
• 00843511111854 - Omnia Medical TiBrid™-SA: 2024-06-20 TiBrid™-SA PLATE, 36mm, L1-L5
• 00843511111861 - Omnia Medical TiBrid™-SA: 2024-06-20 TiBrid™-SA PLATE, 38mm, L1-L5
• 00843511112585 - TiBrid-SA: 2024-06-20 TiBrid-SA Half Moon Inserter (Custom)