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Curad

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
CURAD FDA UDI
Generic Name
Limb immobilization/support skin adhesive tape FDA UDI
Device Name
TAPE,ELASTIC,FOAM,CURAD,4X5.5YD,LF,18/C FDA UDI
Model / Reference
NON270604 FDA UDI
Description
TAPE,ELASTIC,FOAM,CURAD,4X5.5YD,LF,18/C FDA UDI

Identifiers

Catalog Number
NON270604 FDA UDI
Primary DI / UDI-DI
00197344099040 FDA UDI
FDA Product Code
KGX FDA UDI
GMDN Term
Limb immobilization/support skin adhesive tape 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

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

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

Yes

FDA UDI

Category: Limb immobilization/support skin adhesive tape

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

Similar devices

Also classified as Limb immobilization/support skin adhesive tape.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 94091db5-e209-4d6a-9565-89484171fafb 35 fields · synced May 30, 2026