Phoenix Wound Matrix

GUDID 20852513007083

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
Primary Device ID20852513007083
NIH Device Record Key3e94bfe5-0db4-4d6e-b7f8-3e9d15b751b1
Commercial Distribution StatusIn Commercial Distribution
Brand NamePhoenix Wound Matrix
Version Model NumberFG-0013
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 Dimensions

Width1.5 Centimeter
Length2 Centimeter
Width1.5 Centimeter
Length2 Centimeter
Width1.5 Centimeter
Length2 Centimeter
Width1.5 Centimeter
Length2 Centimeter
Width1.5 Centimeter
Length2 Centimeter
Width1.5 Centimeter
Length2 Centimeter
Width1.5 Centimeter
Length2 Centimeter
Width1.5 Centimeter

Operating and Storage Conditions

Storage Environment TemperatureBetween 0 Degrees Celsius and 30 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 30 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 30 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 30 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 30 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 30 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 30 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 30 Degrees Celsius

Device Identifiers

Device Issuing AgencyDevice ID
GS100852513007089 [Primary]
GS110852513007086 [Package]
Contains: 00852513007089
Package: Shelf Box [1 Units]
In Commercial Distribution
GS120852513007083 [Package]
Contains: 10852513007086
Package: Case [5 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FRODressing, Wound, Drug

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2020-05-06
Device Publish Date2019-08-22

On-Brand Devices [Phoenix Wound Matrix]

00852513007041FG-0004
00852513007034FG-0003
00852513007027FG-0002
00852513007010FG-0001
20852513007090FG-0014
20852513007083FG-0013
20852513007076FG-0006
20852513007069FG-0005

Trademark Results [Phoenix Wound Matrix]

Mark Image

Registration | Serial
Company
Trademark
Application Date
PHOENIX WOUND MATRIX
PHOENIX WOUND MATRIX
87781650 not registered Dead/Abandoned
Renovoderm
2018-02-02

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