Dover

FDA UDI

Class II (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name: Dover FDA UDI
Generic Name: Indwelling urethral catheterization kit, adult FDA UDI
Device Name: DOVER VINYL URETHRAL CATHETER, SMOOTH ROUNDED TIP, 5 G LUBRICATING JELLY, 14 FR (4.7 MM) FDA UDI
Model / Reference: 2540 FDA UDI
Description: DOVER VINYL URETHRAL CATHETER, SMOOTH ROUNDED TIP, 5 G LUBRICATING JELLY, 14 FR (4.7 MM) FDA UDI

Identifiers

Catalog Number: 2540- FDA UDI
Primary DI / UDI-DI: 10192253027761 FDA UDI
FDA Product Code: GBM FDA UDI
GMDN Term: Indwelling urethral catheterization kit, adult FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 876.5130 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

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Indwelling urethral catheterization kit, adult

Dover by Cardinal Health 200, LLC — Class II — 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 II	Pending data

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Manufacturer

Manufacturer: Cardinal Health 200, LLC

Sources (1)

FDA UDI ea7c5c1b-ec85-4d08-a246-a5a2da977cae 34 fields · synced Jun 8, 2026