FDA Device Establishments · JSON-LD · Markdown
FEI 3046440169 · Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device · Status: Active
| FEI Number | 3046440169 |
|---|---|
| Owner / Operator | Shenzhen Anker Medical Devices Co., Ltd. (#10096260) |
| Address | Room 1601, 16F, Building 1, Runzhi R&D Center, No. 5, Runfang Road, Area 70, Xingdong Community, Xin'an Sub-district, Bao'an District, Shenzhen Guangdong, 518101, CN |
| Mandatory US Agent | MEDRIGHT TECH INC |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | QUG |
| Regulation § (21 CFR) | 874.3305 |
Source: openFDA. Public-domain (CC0).