FDA Device Establishments · JSON-LD · Markdown
FEI 3027519599 · Manufacture Medical Device · Status: Active
| FEI Number | 3027519599 |
|---|---|
| Owner / Operator | Hangzhou AllTest Biotech Co.,Ltd (#10050156) |
| Address | #383, Qiaoxin Road, Xiasha Street, Qiantang District, Hangzhou Zhejiang, 310018,, CN |
| Mandatory US Agent | ACESO LABORATORIES INC. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 23 |
| Product codes (top 20) | DIS, NGM, DJG, LFG, PTH, DNK, LCM, NGL, NFT, DKZ, NFV, NGG, PTG, DJC, NFW, QAW, NGI, NFY, LDJ, JXM |
| Regulation § (21 CFR) | 862.3150, 862.3650, 862.3910, 862.3640, 862.3100, 862.3170, 862.3610, 862.3620, 862.3870, 862.3250 |
| Proprietary names | One Step Morphine (MOP) Urine Test Strip; Multi-Drug Rapid Test Panel With or without Adulteration (Urine); VeriCheck Drug Test Cup (Urine); Citest Multiplex DOA Test Cup (Urine); Rapid Response Drug Screening Cup w/wo Adulteration (Urine); Discover Multi-Drug Rapid Test Cup (Urine); One Step Cocaine (COC) Urine Test Strip; AllTest Single and Multi-Drug Rapid Test Cup; AllTest Single Drug Home Rapid Test Dipstick; AllTest Single and Multi-Drug Rapid Test Panel With Adulteration |
Source: openFDA. Public-domain (CC0).