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Curad

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Curad FDA UDI
Generic Name
Gauze strip, non-antimicrobial FDA UDI
Device Name
GAUZE,PACKING STRIP,PLAIN,1/4"X5YD,STRL FDA UDI
Model / Reference
NON265145 FDA UDI
Description
GAUZE,PACKING STRIP,PLAIN,1/4"X5YD,STRL FDA UDI

Identifiers

Catalog Number
NON265145 FDA UDI
Primary DI / UDI-DI
10888277690158 FDA UDI
FDA Product Code
NAB FDA UDI
GMDN Term
Gauze strip, non-antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4014 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

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Gauze strip, non-antimicrobial

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

Similar devices

Also classified as Gauze strip, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e5f4bc2e-58c9-460a-bdfb-b0121b71e73b 35 fields · synced May 30, 2026