# HANS RUDOLPH, INC.

FEI: 1922553
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: HANS RUDOLPH, INC. (#1922553)

Address: 8325 COLE PKWY, Shawnee, KS, US



## Products

Total registered: 1
Top product codes: BXW
Regulation §: 868.1870

Proprietary names: RUDOLPH CALIBRATED VARIABLE VOLUME, RUDOLPH F. R. C. CALIBRATION AID, RUDOLPH CALIBRATED SUPER SYRINGE

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%221922553%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=1922553