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Dover

FDA UDI

Class I (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Dover FDA UDI
Generic Name
Midstream urine specimen container IVD FDA UDI
Device Name
Midstream Specimen Catch Kit with Funnel,Castile Soap Towelettes FDA UDI
Model / Reference
2040SA FDA UDI
Description
Midstream Specimen Catch Kit with Funnel,Castile Soap Towelettes FDA UDI

Identifiers

Catalog Number
2040SA FDA UDI
Primary DI / UDI-DI
10884521008274 FDA UDI
FDA Product Code
FMH FDA UDI
GMDN Term
Midstream urine specimen container IVD 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Midstream urine specimen container IVD

Dover by Cardinalhealth — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Midstream urine specimen container IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI 268e84bc-357a-42a0-adc8-5b72717a6aab 36 fields · synced May 30, 2026