FDA Device Establishments · JSON-LD · Markdown
FEI 3016837106 · Manufacture Medical Device · Status: Active
| FEI Number | 3016837106 |
|---|---|
| Owner / Operator | BioTeke Corporation (Wuxi) Co., Ltd (#10071745) |
| Address | No. 90, Huiming Road, Huishan, Wuxi City Jiangsu, 214000, CN |
| Mandatory US Agent | E&E High Tech Solution, Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 10 |
| Product codes (top 20) | NGM, NFV, NGL, NFY, NFT, PTH, QAW, NFW, PTG, NGG |
| Regulation § (21 CFR) | 862.3170, 862.3650, 862.3250, 862.3100, 862.3150, 862.3910, 862.3870, 862.3620, 862.3610 |
| Proprietary names | BioTeke® Multi-Drug Urine Test Cup |
Source: openFDA. Public-domain (CC0).