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 One Step Cup - AMP1000 BAR300 BUP10 BZO300 COC300 MDMA500 MTD300 MET1000 OPI2000 OXY100 THC50 TCA1000 FDA UDI
- Model / Reference
- D12.21-1V FDA UDI
- Description
- Rapid Response Multi-Drug One Step Cup - AMP1000 BAR300 BUP10 BZO300 COC300 MDMA500 MTD300 MET1000 OPI2000 OXY100 THC50 TCA1000 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00722066004722 FDA UDI
- 510(k) Number
- K180349 FDA UDI
- FDA Product Code
- NGG FDA UDINFT FDA UDINFV FDA UDINFW FDA UDINFY FDA UDINGL FDA UDINGM FDA UDIPTG FDA UDIPTH FDA UDIQAW 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 UDI862.3100 FDA UDI862.3170 FDA UDI862.3870 FDA UDI862.3250 FDA UDI862.3650 FDA UDI862.3620 FDA UDI862.3150 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
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.
- OneScreen — AMERICAN SCREENING, L.L.C. · U
- Identify® Diagnostics Drug Test Cards — MEDICAL DISTRIBUTION GROUP INC · Class II
- Healgen (Private Label) - 264 — Confirm Biosciences LLC · Class II
- STATDIP® — MICRO DISTRIBUTING, L.C · Class II
- STATDIP® — MICRO DISTRIBUTING, L.C · Class II
- Precision Plus — AMERICAN SCREENING, L.L.C. · Class II
- DrugCheck — Express Diagnostic Int'l, Inc. · Class II
- QuickProfile™ THC Test Strip — LumiQuick Diagnostics, Inc. · Class II
Cleared under the same submission
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 ddbaaf79-f09b-4f07-9cd6-10e1b1d70df2 34 fields · synced Jun 7, 2026