AccessGUDID - DEVICE: Aurix Eight Pack Kit (10852714003146)

GUDID

Device Identifier (DI) Information

Brand Name: Aurix Eight Pack Kit
Version or Model: AUSP-08
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: Nuo Therapeutics, Inc.

Primary DI Number: 10852714003146
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 118447207 *Terms of Use

Device Description: Aurix Eight Pack Kit Case of 8 Wound Dressing Kits and 8 Reagent Kits with 010512 Aurix Eight Pack Kit Label

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	Yes
Prescription Use (Rx):	No
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
34059	Wound dressing kit, medicated	A collection of instruments, dressings, and pharmaceuticals intended to be used to dress a wound. Items typically include scissors, forceps, gauze, cotton-tip applicators, and antiseptics. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
PMQ	Peripheral Blood Processing Device For Wound Management

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
BK060007	0

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 2b15f01a-88e1-4c71-b020-2cde1f8afe90
Public Version Date: November 28, 2022
Public Version Number: 5
DI Record Publish Date: September 30, 2016