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Rapid Response

FDA UDI

Class II (US FDA UDI)

by BTNX Inc

Identity

Trade Name
Rapid Response FDA UDI
Generic Name
Multiple drugs of abuse IVD, kit, rapid ICT, clinical FDA UDI
Device Name
One Step DOA Cup MOR 2000 (Urine) (D10.1)- COC300 AMP1000 MET1000 THC50 MTD300 OPI2000 PCP25 BAR300 BZO300 TCA1000 FDA UDI
Model / Reference
D10.1-1V FDA UDI
Description
One Step DOA Cup MOR 2000 (Urine) (D10.1)- COC300 AMP1000 MET1000 THC50 MTD300 OPI2000 PCP25 BAR300 BZO300 TCA1000 FDA UDI

Identifiers

Primary DI / UDI-DI
10722066008055 FDA UDI
510(k) Number
K180349 FDA UDI
FDA Product Code
NGI FDA UDI
NFY FDA UDI
NGL FDA UDI
PTG FDA UDI
NFT FDA UDI
NFW FDA UDI
NFV FDA UDI
NGG FDA UDI
GMDN Term
Multiple drugs of abuse IVD, kit, rapid ICT, clinical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.3640 FDA UDI
862.3250 FDA UDI
862.3650 FDA UDI
862.3620 FDA UDI
862.3100 FDA UDI
862.3870 FDA UDI
862.3170 FDA UDI
862.3610 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

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: Multiple drugs of abuse IVD, kit, rapid ICT, clinical

Rapid Response by BTNX Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple drugs of abuse 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

Manufacturer
BTNX Inc

Sources (1)

  • FDA UDI 1edaf6a1-241c-4568-aecf-8623316e6dfc 34 fields · synced Jun 1, 2026