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BluRapids™

FDA UDI

Class II (US FDA UDI)

by Mercedes Medical Llc

Identity

Trade Name
BluRapids™ FDA UDI
Generic Name
Cannabinoid/cannabinoid metabolite IVD, kit, rapid ICT, clinical FDA UDI
Device Name
BlueRapids CLIA Waived Drug Cup; 5-Panal AMP/COC/PCP/OPI2000/THC FDA UDI
Model / Reference
TNR MM5CPCP FDA UDI
Description
BlueRapids CLIA Waived Drug Cup; 5-Panal AMP/COC/PCP/OPI2000/THC FDA UDI

Identifiers

Catalog Number
TNR MM5CPCP FDA UDI
Primary DI / UDI-DI
00850011007020 FDA UDI
510(k) Number
K153050 FDA UDI
FDA Product Code
LDJ FDA UDI
DNK FDA UDI
LCM FDA UDI
DIO FDA UDI
DKZ FDA UDI
GMDN Term
Cannabinoid/cannabinoid metabolite IVD, kit, rapid ICT, clinical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.3870 FDA UDI
862.3640 FDA UDI
862.3250 FDA UDI
862.3100 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

No

FDA UDI

Convenience Kit

No

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: Cannabinoid/cannabinoid metabolite IVD, kit, rapid ICT, clinicalCocaine/cocaine metabolite IVD, kit, rapid ICT, clinicalAmphetamine-specific IVD, kit, rapid ICT, clinicalPhencyclidine (PCP) IVD, kit, rapid ICT, clinical

BluRapids™ by Mercedes Medical Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Morphine/morphine metabolite IVD, kit, rapid ICT, clinical.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9cee183c-73bd-4457-8d51-c98949659879 37 fields · synced May 30, 2026