Phoenix Wound Matrix Fenestrated FG-0023

GUDID 00852513007171

NANOFIBER SOLUTIONS, INC.

Synthetic nanofiber barrier dressing Synthetic nanofiber barrier dressing Synthetic nanofiber barrier dressing Synthetic nanofiber barrier dressing Synthetic nanofiber barrier dressing Synthetic nanofiber barrier dressing Synthetic nanofiber barrier dressing Synthetic nanofiber barrier dressing Synthetic nanofiber barrier dressing Synthetic nanofiber barrier dressing Synthetic nanofiber barrier dressing Synthetic nanofiber barrier dressing Synthetic nanofiber barrier dressing Synthetic nanofiber barrier dressing Synthetic nanofiber barrier dressing

Primary Device ID	00852513007171
NIH Device Record Key	123d59bb-e739-4d14-876c-6ef0b75b0e68
Commercial Distribution Status	In Commercial Distribution
Brand Name	Phoenix Wound Matrix Fenestrated
Version Model Number	FG-0023
Catalog Number	FG-0023
Company DUNS	830384223
Company Name	NANOFIBER SOLUTIONS, 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	false
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	00852513007171 [Primary]

FDA Product Code

FRO	Dressing, Wound, Drug

Sterilization

Steralize Prior To Use	false
Device Is Sterile	true

Device Entry Metadata

Public Version Status	New
Device Record Status	Published
Public Version Number	1
Public Version Date	2022-04-06
Device Publish Date	2022-03-29

On-Brand Devices [Phoenix Wound Matrix Fenestrated]

00852513007201	FG-0026
00852513007195	FG-0025
00852513007188	FG-0024
00852513007171	FG-0023
00852513007164	FG-0022
00852513007157	FG-0021