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ElectroFiber 3D Matrix

FDA UDI

Class U (US FDA UDI)

by Nanofiber Solutions Llc

Identity

Trade Name
ElectroFiber 3D Matrix FDA UDI
Generic Name
Synthetic nanofiber barrier dressing FDA UDI
Model / Reference
FG-0061 FDA UDI

Identifiers

Catalog Number
EF3D-1020 FDA UDI
Primary DI / UDI-DI
00852513007362 FDA UDI
FDA Product Code
FRO FDA UDI
QSZ 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

ElectroFiber 3D Matrix 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 3e9798db-b669-49a2-928e-165068ff0fd6 33 fields · synced Jun 6, 2026