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Curad

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
CURAD FDA UDI
Generic Name
Wound dressing kit, medicated FDA UDI
Device Name
CURAD, SOOTHEPLUS A&H WC KIT, 25PCS FDA UDI
Model / Reference
CURVPACK1 FDA UDI
Description
CURAD, SOOTHEPLUS A&H WC KIT, 25PCS FDA UDI

Identifiers

Catalog Number
CURVPACK1 FDA UDI
Primary DI / UDI-DI
00193489001832 FDA UDI
FDA Product Code
OJJ FDA UDI
GMDN Term
Wound dressing kit, medicated FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4022 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

Yes

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: Wound dressing kit, medicated

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

Similar devices

Also classified as Wound dressing kit, medicated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 72071211-2175-4f3d-9265-fcd8f70a94f7 35 fields · synced May 30, 2026