FDA Device Establishments · JSON-LD · Markdown
FEI 3002808188 · Manufacture Medical Device · Status: Active
| FEI Number | 3002808188 |
|---|---|
| Owner / Operator | STORZ MEDICAL AG (#9028780) |
| Address | LOHSTAMPFESTRASSE 8, TAEGERWILEN Thurgau, 8274, CH |
| Mandatory US Agent | STORZ MEDICAL AMERICA INC. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | ISA |
| Regulation § (21 CFR) | 890.5660 |
| Proprietary names | MASTERPULS R-SW100; CHATTANOOGA Mobile 2 RPW USA; MASTERPULS ONE; D-ACTOR 200; D-ACTOR 50; D-ACTOR 100; DUOLITH SD1 R-SW; MASTERPULS MP100; MASTERPULS icon |
Source: openFDA. Public-domain (CC0).