Cardinal Health

FDA UDI

Class I (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name: CARDINAL HEALTH FDA UDI
Generic Name: Pressure bandage, non-latex, single-use FDA UDI
Device Name: ELASTIC BANDAGE 4INX5.8YD STERILE LATEX FREE WITH VELCRO CLOSURE INDIVIDUALLY WRAPPED PEEL POUCH FDA UDI
Model / Reference: 23593-14LF FDA UDI
Description: ELASTIC BANDAGE 4INX5.8YD STERILE LATEX FREE WITH VELCRO CLOSURE INDIVIDUALLY WRAPPED PEEL POUCH FDA UDI

Identifiers

Catalog Number: 23593-14LF FDA UDI
Primary DI / UDI-DI: 50192253064924 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: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size: Width — 4 Inch FDA UDI
Length — 5.8 Yard FDA UDI

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

Cardinal Health by Cardinal Health 200, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Cardinal Health 200, LLC

Sources (1)

FDA UDI a435ab1a-5798-412f-9811-7c5617480ede 35 fields · synced Jun 8, 2026