Dr Jean Bausch G M B H Co Kg

FDA Filings

This page includes the latest FDA filings for Dr Jean Bausch G M B H Co Kg. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)

• Registration Number: 8010224
• FEI Number: 3004138471
• Name: David Lennarz
• Owner & Operator: Dr. Jean Bausch GmbH & Co. KG
• Contact Address: Oskar-Schindler-Strasse 4 ; Cologne DE-NW Nordrhein-Westfalen D-50769 DE
• US Agent:
  • David Lennarz
  • Registrar Corp
  • 757 2240177
  • 757 2240179
  • david.lennarz@registrarcorp.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 144 Research Drive ; Hampton, VA 23666 US
• Establishment Type: Manufacture Medical Device

FDA Filings

Device Company	Device	Date
GUDID E210BK1450 Dr. Jean Bausch GmbH & Co. KG	Arti-Fol® Approximal Contact Forceps	2020-01-13
GUDID E210BK1440 Dr. Jean Bausch GmbH & Co. KG	Arti-Fol®-Forceps "SteriSlide"	2020-01-13
GUDID E210BK1430 Dr. Jean Bausch GmbH & Co. KG	FIX-CLIP	2020-01-13
GUDID E210BK1420 Dr. Jean Bausch GmbH & Co. KG	Articulating Paper Forceps "Miller"	2020-01-13
GUDID E210BK1330 Dr. Jean Bausch GmbH & Co. KG	Paper-Forceps curved	2020-01-13
GUDID E210BK14008 Dr. Jean Bausch GmbH & Co. KG	Bausch Y-Holder	2019-12-30
GUDID E210BK13209 Dr. Jean Bausch GmbH & Co. KG	Arti-Fol®-Forceps straight, longitudinal groove	2019-12-30
EFK David Lennarz [Dr. Jean Bausch GmbH & Co. KG]	Bausch Articulating Paper Forceps	2013-06-27
EFK David Lennarz [Dr. Jean Bausch GmbH & Co. KG]	Bausch Arti-Fol Forceps	2013-06-27
EFH David Lennarz [Dr. Jean Bausch GmbH & Co. KG]	OccluSense	1989-06-26
EFH David Lennarz [Dr. Jean Bausch GmbH & Co. KG]	ARTICULATING PAPERS	1989-06-26