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DeRoyal

FDA UDI

Class U (US FDA UDI)

by Deroyal Industries, Inc.

Identity

Trade Name
DeRoyal FDA UDI
Generic Name
Wound-nonadherent dressing, permeable, antimicrobial FDA UDI
Device Name
Dermanet Ag 4 x 4 (10cm x 10cm) FDA UDI
Model / Reference
46-DN44-1 FDA UDI
Description
Dermanet Ag 4 x 4 (10cm x 10cm) FDA UDI

Identifiers

Catalog Number
46-DN44-1 FDA UDI
Primary DI / UDI-DI
00749756646659 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Wound-nonadherent dressing, permeable, antimicrobial 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: Wound-nonadherent dressing, permeable, antimicrobial

DeRoyal by Deroyal Industries, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wound-nonadherent dressing, permeable, antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8657b3bd-3494-42f9-9cea-6be168ef36ff 34 fields · synced Jun 8, 2026