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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
Elastic Bandage with Removable Clip FDA UDI
Model / Reference
4422 FDA UDI
Description
Elastic Bandage with Removable Clip FDA UDI

Identifiers

Catalog Number
4422 FDA UDI
Primary DI / UDI-DI
10884521124448 FDA UDI
FDA Product Code
FQM FDA UDI
GMDN Term
Pressure bandage, non-latex, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5075 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Width — 2 Inch FDA UDI

Curity by Cardinalhealth — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI 6c2b8682-0fd9-440f-90ec-3c93d9ca424a 37 fields · synced May 30, 2026