Centrio

GUDID 00852714003330

Nuo Therapeutics, Inc.

Wound dressing kit, medicated

• Primary Device ID: 00852714003330
• NIH Device Record Key: 078b9651-8f87-4e20-b0e4-51b344b92e23
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Centrio
• Version Model Number: Reagent Kit
• Company DUNS: 118447207
• Company Name: Nuo Therapeutics, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00852714003330 [Primary]

FDA Product Code

• PMQ: Peripheral Blood Processing Device For Wound Management

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-09-09
• Device Publish Date: 2025-09-01

On-Brand Devices [Centrio]

• 00852714003347: Office Wound Dressing Kit
• 00852714003330: Reagent Kit
• 00852714003323: Wound Dressing Kit
• 00852714003316: Centrio Multifly Needle - 4 Pack
• 00852714003309: Centrio PRP System - Office Single Kit
• 00852714003293: Centrio PRP System - 10 Kits
• 00852714003286: Centrio PRP System - 5 Kits
• 00852714003279: Centrio PRP System- Single Kit