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Curity

FDA UDI

Class I (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Curity FDA UDI
Generic Name
Pressure bandage, non-latex, single-use FDA UDI
Device Name
Stretch Bandage FDA UDI
Model / Reference
2230 FDA UDI
Description
Stretch Bandage FDA UDI

Identifiers

Catalog Number
2230 FDA UDI
Primary DI / UDI-DI
10884527015627 FDA UDI
FDA Product Code
ITG FDA UDI
GMDN Term
Pressure bandage, non-latex, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3025 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

Dimensions & Sizes

Size
Width — 1 Inch FDA UDI
Length — 75 Inch FDA UDI

Category: Pressure bandage, non-latex, single-use

Curity is a stretch bandage device that provides comfortable and effective support for various medical applications, including physical therapy, wound care, and athletic injuries. This single-use device features a non-latex material, sterilization via autoclaving or gamma radiation, and is designed for use in the home or healthcare facility.

Similar devices

Also classified as Pressure bandage, non-latex, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI 75df01b0-915b-4683-b74e-95ed067cfee8 37 fields · synced Jul 7, 2026