Gebruder Renggli Ag

FDA Filings

This page includes the latest FDA filings for Gebruder Renggli Ag. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3009538961
FEI Number3009538961
NameCharles Cathlin
Owner & OperatorGebruder Renggli AG
Contact AddressSchweizerbildstrasse 57 CH-8200
Schaffhausen CH-SH Schaffhausen 8200 CH
Official Correspondent
  • Caroline Mueller
  • 041-52-6445514-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address15807 Glacier Ct
North Potomac, MD 20878 US
Establishment Type
  • Manufacture Medical Device
  • Manufacture Medical Device for Another Party (Contract Manufacturer)

FDA Filings

Device
Company
DeviceDate
Charles Cathlin [Gebruder Renggli AG]
Schlauchset, Absaugung, DS2020-04-15
Charles Cathlin [Gebruder Renggli AG]
Schlauchset, Absaugung, BS2020-04-15
Charles Cathlin [Gebruder Renggli AG]
Schlauchset, Spuelung, PC2018-11-28
Charles Cathlin [Gebruder Renggli AG]
Schlauchset, Spuelung, FC2018-11-28
Charles Cathlin [Gebruder Renggli AG]
Schlauchset, Spuelung, CV2018-11-28
Charles Cathlin [Gebruder Renggli AG]
Schlauchset, Absaugung, DS2018-11-28
Charles Cathlin [Gebruder Renggli AG]
Schlauchset, Absaugung, BS2018-11-28
Charles Cathlin [Gebruder Renggli AG]
C-MAS Videolaryngoskop MAC #42018-11-28
Charles Cathlin [Gebruder Renggli AG]
C-MAS Videolaryngoskop D-BLADE2018-11-28
Charles Cathlin [Gebruder Renggli AG]
C-MAS S Videolaryngoskop MAC #32018-11-28
Charles Cathlin [Gebruder Renggli AG]
Cavifil Injector2012-02-08
Charles Cathlin [Gebruder Renggli AG]
OptraSculpt2012-02-08

Related Finance Registrations
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.