Dover

FDA UDI

Class I (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name: Dover FDA UDI
Generic Name: Urine strainer FDA UDI
Device Name: Calculi Strainer FDA UDI
Model / Reference: 2110SA FDA UDI
Description: Calculi Strainer FDA UDI

Identifiers

Catalog Number: 2110SA FDA UDI
Primary DI / UDI-DI: 50192253051429 FDA UDI
FDA Product Code: FMH FDA UDI
GMDN Term: Urine strainer FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 864.3250 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

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

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Total Volume — 2 Fluid Ounce FDA UDI

Category: Urine strainer

Dover 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 00ac0e82-7e5a-4e76-8b1c-12c09fac7a9a 35 fields · synced Jun 8, 2026