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Aurix Five Pack Kit

FDA UDI

Class II (US FDA UDI)

by Nuo Therapeutics, Inc.

Identity

Trade Name
Aurix Five Pack Kit FDA UDI
Generic Name
Wound dressing kit, medicated FDA UDI
Device Name
Aurix Five Pack Kit Case of 5 Wound Dressing Kits and 5 Reagent Kits with 010503 Aurix Five Pack Kit Label FDA UDI
Model / Reference
AUSP-05 FDA UDI
Description
Aurix Five Pack Kit Case of 5 Wound Dressing Kits and 5 Reagent Kits with 010503 Aurix Five Pack Kit Label FDA UDI

Identifiers

Primary DI / UDI-DI
10852714003139 FDA UDI
FDA Product Code
PMQ FDA UDI
GMDN Term
Wound dressing kit, medicated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.9245 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Wound dressing kit, medicated

Aurix Five Pack Kit by Nuo Therapeutics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wound dressing kit, medicated.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 67b087e0-04dd-45e1-96df-160473faf766 34 fields · synced May 30, 2026