# STORZ MEDICAL AG

FEI: 3002808188
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: STORZ MEDICAL AG (#9028780)

Address: LOHSTAMPFESTRASSE 8, TAEGERWILEN Thurgau, 8274, CH

Mandatory US Agent: STORZ MEDICAL AMERICA INC.

## Products

Total registered: 1
Top product codes: ISA
Regulation §: 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: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223002808188%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3002808188