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LetsGetChecked Urine Sample Collection Kit (SM02)

FDA UDI

Class II (US FDA UDI)

by Privapath Diagnostics Limited

Identity

Trade Name
LetsGetChecked Urine Sample Collection Kit (SM02) FDA UDI
Generic Name
Urine specimen collection kit IVD FDA UDI
Device Name
A collection of noninvasive devices intended to be used for the collection, and preservation and/or transport, of a urine specimen for culture, analysis, and/or other investigation. FDA UDI
Model / Reference
UO305, UO01S FDA UDI
Description
A collection of noninvasive devices intended to be used for the collection, and preservation and/or transport, of a urine specimen for culture, analysis, and/or other investigation. FDA UDI

Identifiers

Catalog Number
UO305, UO01S FDA UDI
Primary DI / UDI-DI
00850024881327 FDA UDI
FDA Product Code
QYA FDA UDI
GMDN Term
Urine specimen collection kit IVD FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.3385 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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Urine specimen collection kit IVD

LetsGetChecked Urine Sample Collection Kit (SM02) by Privapath Diagnostics Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Urine specimen collection kit IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI eae6cb6c-c7f5-44b3-806e-b99438abdd47 34 fields · synced Jun 8, 2026