FDA Device Establishments · JSON-LD · Markdown
FEI 3026317086 · Manufacture Medical Device · Status: Active
| FEI Number | 3026317086 |
|---|---|
| Owner / Operator | Deepintec Scientific Co., Ltd (#10093943) |
| Address | Building No. 4, 18Kechuang 10th Street, DBA, Beijing, Beijing, 100176, CN |
| Mandatory US Agent | Arbor Endovascular |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 2 |
| Product codes (top 20) | DQX, MOF |
| Regulation § (21 CFR) | 870.1330 |
| Proprietary names | Willow 24 Guidewire |
Source: openFDA. Public-domain (CC0).