Breitfeld Schliekert G M B H

FDA Filings

This page includes the latest FDA filings for Breitfeld Schliekert G M B H. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3012576645
FEI Number3012576645
NameBREITFELD & SCHLIEKERT GMBH
Owner & OperatorBreitfeld & Schliekert GmbH
Contact AddressMax-Planck-Str. 30
Karben DE-HE Hessen 61184 DE
Official Correspondent
  • Alexandra Szanto
  • 49-603-9993-33
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressMax-Planck-Str. 30
Karben Hessen, 61184 DE
Establishment Type
  • Manufacture Medical Device
  • Export Device to the United States But Perform No Other Operation on Device



FDA Filings

Device
Company
DeviceDate
BREITFELD & SCHLIEKERT GMBH
WAYCOOL FLIPUPS2016-09-08
BREITFELD & SCHLIEKERT GMBH
Hilco Vision2016-09-08

Related Finance Registrations
U.S. Import Records [external site]
Import IDShipmentCargo DescriptionQuantity
2020091135899Stadersand,Federal Republic of Germany -> New York/Newark Area, Newark, New JerseyOPTICAL GOODSHS CODE 39191080 39231090 39269097 90039000 900410912 CTN
2020091031067Stadersand,Federal Republic of Germany -> New York/Newark Area, Newark, New JerseyOPTICAL GOODSHS CODE 39191080 39231090 39269097 90039000 900410912 CTN
2020090539333Stadersand,Federal Republic of Germany -> New York/Newark Area, Newark, New JerseyOPTICAL GOODSHS CODE 39191080 39231090 39269097 90039000 900410912 CTN
2020082655665Stadersand,Federal Republic of Germany -> New York/Newark Area, Newark, New JerseyOPTICAL GOODSHS CODE 39191080 39231090 39269097 90039000 900410912 CTN

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