FDA Device Establishments · JSON-LD · Markdown
FEI 3013024191 · Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3013024191 |
|---|---|
| Owner / Operator | Urogen Pharma Ltd. (#10055966) |
| Address | 9 Ha'Ta'asiya Street, Ra'anana Central, 4365007, IL |
| Mandatory US Agent | Urogen Pharma Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | OHR |
| Regulation § (21 CFR) | 876.5130 |
| Proprietary names | Ureteral Catheter Administration Kit; Intravesical Administation Kit |
Source: openFDA. Public-domain (CC0).