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Dover

FDA UDI

Class II (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
Dover FDA UDI
Generic Name
Intermittent urethral drainage catheter, non-antimicrobial, reusable FDA UDI
Device Name
DOVER VINYL URETHRAL CATHETER, INTEGRAL FUNNEL, SMOOTH ROUNDED TIP, 8 FR (2.7 MM) FDA UDI
Model / Reference
400608 FDA UDI
Description
DOVER VINYL URETHRAL CATHETER, INTEGRAL FUNNEL, SMOOTH ROUNDED TIP, 8 FR (2.7 MM) FDA UDI

Identifiers

Catalog Number
400608 FDA UDI
Primary DI / UDI-DI
10192253029079 FDA UDI
FDA Product Code
KOD FDA UDI
GMDN Term
Intermittent urethral drainage catheter, non-antimicrobial, reusable 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

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

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
Catheter Gauge — 8 French FDA UDI

Category: Intermittent urethral drainage catheter, non-antimicrobial, reusable

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

Similar devices

Also classified as Intermittent urethral drainage catheter, non-antimicrobial, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinal Health 200, LLC

Sources (1)

  • FDA UDI c25fbd73-d80a-4ff3-abfb-ecd53118e9b8 35 fields · synced Jun 8, 2026