← Back to catalogue

Curad

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
CURAD FDA UDI
Generic Name
Adhesive bandage FDA UDI
Device Name
CURAD, FAMILY PACK W DECO, 175CT FDA UDI
Model / Reference
CURVPACK9 FDA UDI
Description
CURAD, FAMILY PACK W DECO, 175CT FDA UDI

Identifiers

Catalog Number
CURVPACK9 FDA UDI
Primary DI / UDI-DI
00193489027221 FDA UDI
FDA Product Code
KGX FDA UDI
GMDN Term
Adhesive bandage FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5240 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

Yes

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Adhesive bandage

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

Similar devices

Also classified as Adhesive bandage.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 41ece4a6-ef59-492b-8fc7-654d72597d2d 35 fields · synced May 30, 2026