Identity
- Trade Name
- Rapid Response FDA UDI
- Generic Name
- Multiple drugs of abuse IVD, kit, rapid ICT, clinical FDA UDI
- Device Name
- Rapid Response Multi Drug Test Panels (COC/AMP/MET/THC/MTD/OPI/OXY/BAR/BZO/TCA) - 25 tests/ kit are for the qualitative detection of Amphetamine, Methamphetamine, Methadone, Opiates, Oxycodone, Barbiturates, Benzodiazepines, Tricyclic Antidepressant, Cocaine and THC metabolites in urine. FDA UDI
- Model / Reference
- D10.6-1P29-25 FDA UDI
- Description
- Rapid Response Multi Drug Test Panels (COC/AMP/MET/THC/MTD/OPI/OXY/BAR/BZO/TCA) - 25 tests/ kit are for the qualitative detection of Amphetamine, Methamphetamine, Methadone, Opiates, Oxycodone, Barbiturates, Benzodiazepines, Tricyclic Antidepressant, Cocaine and THC metabolites in urine. FDA UDI
Identifiers
- Catalog Number
- D10.6-1P29-25 FDA UDI
- Primary DI / UDI-DI
- 00722066003312 FDA UDI
- FDA Product Code
- DJC FDA UDIDJR FDA UDIDJG FDA UDILDJ FDA UDIDIO FDA UDIJXM FDA UDIDIS FDA UDIDKZ FDA UDIQAW FDA UDIPTG FDA UDINGG FDA UDINGL FDA UDINFY FDA UDIPTH FDA UDINFT FDA UDINFV FDA UDINFW FDA UDI
- GMDN Term
- Multiple drugs of abuse IVD, kit, rapid ICT, clinical FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.3610 FDA UDI862.3620 FDA UDI862.3650 FDA UDI862.3870 FDA UDI862.3250 FDA UDI862.3170 FDA UDI862.3150 FDA UDI862.3100 FDA UDI862.3910 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
Yes
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: 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
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Cleared under the same submission
K121065 also covers:
- Rapid Response — BTNX Inc
- Rapid Response — BTNX Inc
- Rapid Response — BTNX Inc
- Rapid Response — BTNX Inc
- Rapid Response — BTNX Inc
- Rapid Response — BTNX Inc
- Rapid Response — BTNX Inc
- Rapid Response — BTNX Inc
- Rapid Response — BTNX Inc
- Rapid Response — BTNX Inc
- Rapid Response — BTNX Inc
- Rapid Response — BTNX Inc
K180349 also covers:
- Discover — AMERICAN SCREENING, L.L.C.
- Discover — AMERICAN SCREENING, L.L.C.
- Discover — AMERICAN SCREENING, L.L.C.
- Discover — AMERICAN SCREENING, L.L.C.
- Discover — AMERICAN SCREENING, L.L.C.
- Discover — AMERICAN SCREENING, L.L.C.
- Discover — AMERICAN SCREENING, L.L.C.
- Discover — AMERICAN SCREENING, L.L.C.
- Discover — AMERICAN SCREENING, L.L.C.
- Discover Plus — AMERICAN SCREENING, L.L.C.
- Discover Plus — AMERICAN SCREENING, L.L.C.
- Discover Plus — AMERICAN SCREENING, L.L.C.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- BTNX Inc
Sources (1)
- FDA UDI 7e3455dc-8376-4d64-abd7-8d57b78fb6ef 35 fields · synced May 30, 2026