# FUJIFILM medwork GmbH

FEI: 3020707080
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: FUJIFILM CORPORATION (#8031568)

Address: Medworkring 1, Hochstadt/Aisch Bavaria, 91315, DE

Mandatory US Agent: FUJIFILM Healthcare Americas Corporation

## Products

Total registered: 1
Top product codes: GCE
Regulation §: 878.4200

Proprietary names: Application Catheter

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223020707080%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3020707080