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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
Urine flowmeter, single-use FDA UDI
Device Name
URINE DRAINAGE BAG WITH 200 ML URINE METER, NEEDLE SAMPLING, DRAIN TUBE FDA UDI
Model / Reference
8000 FDA UDI
Description
URINE DRAINAGE BAG WITH 200 ML URINE METER, NEEDLE SAMPLING, DRAIN TUBE FDA UDI

Identifiers

Catalog Number
8000- FDA UDI
Primary DI / UDI-DI
10884521002180 FDA UDI
FDA Product Code
FFG FDA UDI
GMDN Term
Urine flowmeter, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1800 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

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
Total Volume — 200 Milliliter FDA UDI

Category: Urine flowmeter, single-use

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

Similar devices

Also classified as Urine flowmeter, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f98640a2-60eb-431f-8b69-f6c34a7110e8 36 fields · synced Jun 8, 2026