# MEDNOSBRO GMBH

FEI: 3008593890
Status: Active
Establishment types: Export Device to the United States But Perform No Other Operation on Device
Owner/operator: MEDNOSBRO GmbH (#10041183)

Address: Schuermatt 1, Rudolfstetten Aargau, 8964, CH

Mandatory US Agent: AutomatedMedical Products Corp.

## Products

Total registered: 1
Top product codes: GDI
Regulation §: 878.4800

Proprietary names: REMA Dissector, Articulating Dissector

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223008593890%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3008593890