DrugTect Multi-Drug Rapid Test Cup
DrugTect, 14 Panel Multi-Drug Test Cup, CLIA WAIVED (AMP500, BAR300, BUP10, BZO300, COC150, FYL1, MDMA500, MET500, MOP300, MTD300 OXY100, PCP25, TCA1000, THC50) + (OX, SG, PH) + (NIT, GUL,…
DrugTect, 14 Panel Multi-Drug Test Cup, CLIA WAIVED (AMP500, BAR300, BUP10, BZO300, COC150, FYL1, MDMA500, MET500, MOP300, MTD300 OXY100, PCP25, TCA1000, THC50) + (OX, SG, PH) + (NIT, GUL, CRE) Contents: Test Cups – 100, Package Insert – 1, Adulteration Color Chart – 1, Security Seals → 100. For In Vitro Diagnostics Use
Who Else Makes It
Concentrated in Zhejiang (8), Guangdong (4), Tianjin (1). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Zhejiang Orient Gene Biotech | Huzhou | Zhejiang | Contract manufacturer | 86 |
| Hangzhou Biotest Biotech Co., Ltd. | Hangzhou | Zhejiang | Contract manufacturer | 41 |
| Co-Innovation Biotech Co., Ltd. | Guangzhou | Guangdong | Contract manufacturer | 29 |
| Jcmed Tianjin Import AND Export Co., Ltd. | Tianjin | Tianjin | Manufacturer | 51 |
| Hangzhou AllTest Biotech Co., Ltd. | Hangzhou | Zhejiang | Contract manufacturer | 48 |
| Assure Tech. (Hangzhou) Co., Ltd. | Hangzhou | Zhejiang | Contract manufacturer | 48 |
| Guangzhou Wondfo Biotech Co., Ltd. | Guangzhou | Guangdong | Contract manufacturer | 44 |
| W.h.p.m. Bioresearch & Technology Co., Ltd. | Beijing | Beijing | Manufacturer | 37 |
| Guangzhou Decheng Biotechnology Co., Ltd. | Guangzhou | Guangdong | Complaint-file establishment | 35 |
| Eterbio, Inc. | Zhuhai | Guangdong | Manufacturer | 29 |
| Safecare Biotech(Hangzhou)Co., Ltd. | Huzhou | Zhejiang | Manufacturer | 22 |
| Vivachek Biotech (Hangzhou) Co., Ltd. | Hangzhou, Zhuji | Zhejiang | Contract manufacturer | 21 |
Showing 12 of 16. All 16 manufacturers in China registered for Test, Amphetamine, Over The Counter
Record
| Listed by | Hangzhou AllTest Biotech Co., Ltd., China |
|---|---|
| FDA product code | NFT |
| Device type | Test, Amphetamine, Over The Counter |
| Device class | Class 2 |
| Regulation | 21 CFR 862.3100 |
| Establishment | Contract manufacturer, Manufacturer |
| Record published | 2025-11-15 |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Single use | Yes |
| Over the counter | Yes |
| Label carries | lot or batch number, expiry date |
Catalogue Numbers
| Catalogue number | Size | Per pack | Status |
|---|---|---|---|
| DT-AT12-1-AZ50 | 50 | In distribution | |
| DT-AT12-1-AZ5 | 5 | In distribution | |
| DT-AT12-1-AZ200 | 200 | In distribution | |
| 1 | 5 | In distribution | |
| 1 | In distribution | ||
| DT-AT14-AD6-1-AZ100 | 100 | In distribution | |
| DT-AT12-1-AZ25 | 25 | In distribution | |
| DT-AT14-AD6-1-AZ200 | 200 | In distribution | |
| 1 | In distribution | ||
| DT-AT12-1-AZ100 | 100 | In distribution | |
| DT-AT14-AD6-1-AZ75 | 75 | In distribution | |
| 1 | 5 | In distribution | |
| 1 | 25 | In distribution | |
| DT-AT14-AD6-1-AZ5 | 5 | In distribution | |
| DT-AT12-1-AZ1 | In distribution | ||
| 1 | 2 | In distribution | |
| DT-AT12-1-AZ75 | 75 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Discover Plus | American Screening, L.L.C. | 59 |
| Precision DX | American Screening, L.L.C. | 42 |
| Discover | American Screening, L.L.C. | 32 |
| iScreen™ | Instant Technologies, Inc. | 31 |
| Reveal | American Screening, L.L.C. | 26 |
| Prime Screen | Wondfo USA Co., Ltd. | 20 |
| U-Catch | Shenzhen Bioeasy Biotechnology Co., Ltd. | 19 |
| SAFElife™ | Wondfo USA Co., Ltd. | 18 |
| Precision Plus | American Screening, L.L.C. | 12 |
| Rapid Response | Btnx Inc. | 11 |
| OneScreen | American Screening, L.L.C. | 9 |
| Discover Multi-Drug Test Cup | Hangzhou AllTest Biotech Co., Ltd. | 9 |
Showing 12 of 113. All products under Test, Amphetamine, Over The Counter
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K250727 | 2025-04-04 |
| K244043 | 2025-02-27 |
| K242540 | 2024-09-27 |
| K241428 | 2024-06-17 |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.