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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
BluRapids CLIA Waived Drug Cup; 6 Panel with Adulterants BZO/COC/MET/OPI/OXY/THC FDA UDI
Model / Reference
TNR CDOA262 FDA UDI
Description
BluRapids CLIA Waived Drug Cup; 6 Panel with Adulterants BZO/COC/MET/OPI/OXY/THC FDA UDI

Identifiers

Catalog Number
TNR CDOA262 FDA UDI
Primary DI / UDI-DI
00850011007044 FDA UDI
510(k) Number
K153050 FDA UDI
FDA Product Code
LDJ FDA UDI
DJG FDA UDI
DNK FDA UDI
DJC FDA UDI
DIO FDA UDI
JXM 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
862.3650 FDA UDI
862.3640 FDA UDI
862.3610 FDA UDI
862.3250 FDA UDI
862.3170 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, clinicalMethamphetamine-specific IVD, kit, rapid ICT, clinicalBenzodiazepine group 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 Oxycodone 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 71956ea7-374a-4ade-8981-87dfa713e2cb 37 fields · synced Jun 8, 2026