FDA Device Establishments · JSON-LD · Markdown
FEI 3039020025 · Manufacture Medical Device · Status: Active
| FEI Number | 3039020025 |
|---|---|
| Owner / Operator | Suzhou Zenith Vascular SciTech Limited (#10095913) |
| Address | Ground Floor to 5th Floor, Underground Unit B102, Building 6, Block B, Phase 5, Biobay, No.21 Dongyanli Road, SIP, Suzhou Jiangsu, 215123, CN |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 2 |
| Product codes (top 20) | MOF, DQX |
| Regulation § (21 CFR) | 870.1330 |
| Proprietary names | Zenith Micro Guidewire |
Source: openFDA. Public-domain (CC0).