Aurix Five Pack Kit

GUDID 10852714003139

Aurix Five Pack Kit Case of 5 Wound Dressing Kits and 5 Reagent Kits with 010503 Aurix Five Pack Kit Label

NUO THERAPEUTICS INC

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• Primary Device ID: 10852714003139
• NIH Device Record Key: 67b087e0-04dd-45e1-96df-160473faf766
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Aurix Five Pack Kit
• Version Model Number: AUSP-05
• Company DUNS: 132418851
• 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: true
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	10852714003139 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• BK060007

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: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2021-11-01
• Device Publish Date: 2016-09-30

Devices Manufactured by NUO THERAPEUTICS INC

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• 10852714003139 - Aurix Five Pack Kit: 2021-11-01 Aurix Five Pack Kit Case of 5 Wound Dressing Kits and 5 Reagent Kits with 010503 Aurix Five Pack Kit Label
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