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Curad

FDA UDI

Class U (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
CURAD FDA UDI
Generic Name
Petrolatum non-woven gauze pad FDA UDI
Device Name
DRESSING,GAUZE,OIL EMULSION,CURAD,3"X3" FDA UDI
Model / Reference
CUR250330 FDA UDI
Description
DRESSING,GAUZE,OIL EMULSION,CURAD,3"X3" FDA UDI

Identifiers

Catalog Number
CUR250330 FDA UDI
Primary DI / UDI-DI
10884389113127 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Petrolatum non-woven gauze pad 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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

Yes

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: Petrolatum non-woven gauze pad

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

Similar devices

Also classified as Petrolatum non-woven gauze pad.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e5087be6-398e-416a-a525-2b9d299a7c50 35 fields · synced Jun 8, 2026