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Phoenix Wound Matrix Fenestrated

FDA UDI

Class U (US FDA UDI)

by Nanofiber Solutions Llc

Identity

Trade Name
Phoenix Wound Matrix Fenestrated FDA UDI
Generic Name
Synthetic nanofiber barrier dressing FDA UDI
Model / Reference
FG-0026 FDA UDI

Identifiers

Catalog Number
FG-0026 FDA UDI
Primary DI / UDI-DI
00852513007201 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Synthetic nanofiber barrier dressing FDA UDI

Classification

Device Class
U FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

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

No

FDA UDI

Category: Synthetic nanofiber barrier dressing

Phoenix Wound Matrix Fenestrated by Nanofiber Solutions Llc — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Synthetic nanofiber barrier dressing.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nanofiber Solutions Llc

Sources (1)

  • FDA UDI 3d136e00-b5d0-4dc4-ac4b-74e0e1fc5fa7 33 fields · synced May 30, 2026