# CURATRONIC, LTD.

FEI: 3004938911
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: CURATRONIC, LTD. (#9069104)

Address: 101  HEBRON ROAD, JERUSALEM Central, 9348001, IL

Mandatory US Agent: A. STEIN - REGULATORY AFFAIRS CONSULTING LTD.

## Products

Total registered: 1
Top product codes: IPF
Regulation §: 890.5850

Proprietary names: Biomove 5000

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223004938911%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3004938911