FDA Device Establishments · JSON-LD · Markdown
FEI 3011276773 · Reprocess Single-Use Device Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3011276773 |
|---|---|
| Owner / Operator | STERILMED, INC. (#9030419) |
| Address | 5010 Cheshire Pkwy N Ste 2, Plymouth, MN, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | OWQ |
| Regulation § (21 CFR) | 870.1200 |
| Proprietary names | Reprocessed Ultrasound Catheter |
Source: openFDA. Public-domain (CC0).