Aurix XL

GUDID 00852714003187

Aurix XL is a phlebotomy convenience kit

Nuo Therapeutics, Inc.

Phlebotomy kit

• Primary Device ID: 00852714003187
• NIH Device Record Key: 8f122966-1f65-48af-b14b-1961ecb31ad9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Aurix XL
• Version Model Number: AUXP-2T
• Company DUNS: 118447207
• Company Name: Nuo Therapeutics, 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: 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: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00852714003187 [Primary]

FDA Product Code

• OFM: Phlebotomy Blood Collection Kit

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: 2023-04-04
• Device Publish Date: 2023-03-27

Devices Manufactured by Nuo Therapeutics, Inc.

• 00852714003279 - Centrio: 2025-09-09
• 00852714003286 - Centrio: 2025-09-09
• 00852714003293 - Centrio: 2025-09-09
• 00852714003309 - Centrio: 2025-09-09
• 00852714003316 - Centrio: 2025-09-09
• 00852714003323 - Centrio: 2025-09-09
• 00852714003330 - Centrio: 2025-09-09
• 00852714003347 - Centrio: 2025-09-09