Phoenix Surgical Wound Matrix Fenestrated FG-0052

GUDID 00852513007324

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 Synthetic nanofiber barrier dressing Synthetic nanofiber barrier dressing
Primary Device ID00852513007324
NIH Device Record Key4b1ce1b9-9d70-4a61-928f-0cd37d7a2974
Commercial Distribution StatusIn Commercial Distribution
Brand NamePhoenix Surgical Wound Matrix Fenestrated
Version Model NumberFG-0052
Catalog NumberFG-0052
Company DUNS830384223
Company NameNANOFIBER SOLUTIONS, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100852513007324 [Primary]

FDA Product Code

FRODressing, Wound, Drug

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-02-24
Device Publish Date2023-02-16

On-Brand Devices [Phoenix Surgical Wound Matrix Fenestrated]

00852513007324FG-0052
00852513007003FG-0051

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.