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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 woven gauze pad FDA UDI
Device Name
DRESSING,GAUZE,XERO,CURAD,4"X3 YARD,ST FDA UDI
Model / Reference
CUR253200 FDA UDI
Description
DRESSING,GAUZE,XERO,CURAD,4"X3 YARD,ST FDA UDI

Identifiers

Catalog Number
CUR253200 FDA UDI
Primary DI / UDI-DI
10884389160367 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Petrolatum 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

Yes

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 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 woven gauze pad.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ebac35d8-6b8d-4691-804b-e03ec1bd1b7c 35 fields · synced Jun 8, 2026