FDA Device Establishments · JSON-LD · Markdown
FEI 3009350690 · Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3009350690 |
|---|---|
| Owner / Operator | STRYKER CORP. (#1811755) |
| Address | 1810 W. Drake Dr., Tempe, AZ, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | NLH |
| Regulation § (21 CFR) | 870.1220 |
| Proprietary names | Reprocessed Electrophysiology Catheter |
Source: openFDA. Public-domain (CC0).