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Curad

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Curad FDA UDI
Generic Name
Ankle binder, reusable FDA UDI
Device Name
WRAP,ANKLE,ADJUSTABLE,RETAIL,BLK,4/CS FDA UDI
Model / Reference
CURORT267 FDA UDI
Description
WRAP,ANKLE,ADJUSTABLE,RETAIL,BLK,4/CS FDA UDI

Identifiers

Catalog Number
CURORT267 FDA UDI
Primary DI / UDI-DI
00197344003382 FDA UDI
FDA Product Code
CCX FDA UDI
GMDN Term
Ankle binder, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.6820 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

No

FDA UDI

Category: Ankle binder, reusable

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

Similar devices

Also classified as Ankle binder, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medline Industries, Inc.

Sources (1)

  • FDA UDI 7a488e7d-12d3-4c64-add3-9397e500c2b0 35 fields · synced Jun 8, 2026