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Curad

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Curad FDA UDI
Generic Name
Public face mask, single-use FDA UDI
Device Name
DBD-MASK,RESPIRATOR,N95,CONE STYLE,LF FDA UDI
Model / Reference
CUR24506A FDA UDI
Description
DBD-MASK,RESPIRATOR,N95,CONE STYLE,LF FDA UDI

Identifiers

Catalog Number
CUR24506A FDA UDI
Primary DI / UDI-DI
00888277728724 FDA UDI
FDA Product Code
MSH FDA UDI
GMDN Term
Public face mask, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4040 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Public face mask, single-use

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

Similar devices

Also classified as Public face mask, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f95cf07f-195f-4720-8459-6f9c404cbf28 35 fields · synced Jun 1, 2026