FDA Device Establishments · JSON-LD · Markdown
FEI 1922553 · Manufacture Medical Device · Status: Active
| FEI Number | 1922553 |
|---|---|
| Owner / Operator | HANS RUDOLPH, INC. (#1922553) |
| Address | 8325 COLE PKWY, Shawnee, KS, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | BXW |
| Regulation § (21 CFR) | 868.1870 |
| Proprietary names | RUDOLPH CALIBRATED VARIABLE VOLUME; RUDOLPH F. R. C. CALIBRATION AID; RUDOLPH CALIBRATED SUPER SYRINGE |
Source: openFDA. Public-domain (CC0).