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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
Commode Specimen Collector FDA UDI
Model / Reference
2500SA FDA UDI
Description
Commode Specimen Collector FDA UDI

Identifiers

Catalog Number
2500SA FDA UDI
Primary DI / UDI-DI
10884521008335 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

No

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

Dimensions & Sizes

Size
Total Volume — 800 Milliliter 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 086a863b-bad3-4a9a-911c-b130dfbecce0 37 fields · synced Jun 8, 2026