Alfred Becht G M B H

FDA Filings

This page includes the latest FDA filings for Alfred Becht 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 Number3001251335
FEI Number3001251335
NameALFRED BECHT GMBH
Owner & OperatorAlfred Becht GmbH
Contact AddressCarl-Zeiss-Strasse 16 Baden-Wurttemberg
Offenburg DE-BW Baden-Wurttemberg 77656 DE
Official Correspondent
  • Ulrich A Becht
  • 49-781-60586-0
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressCarl-Zeiss-Strasse 16 Baden-Wurttemberg
Offenburg Baden-Wurttemberg, 77656 DE
Establishment Type
  • Repack or Relabel Medical Device
  • Foreign Private Label Distributor
  • Export Device to the United States But Perform No Other Operation on Device



FDA Filings

Device
Company
DeviceDate
ALFRED BECHT GMBH
EJR - AGENT, POLISHING, ABRASIVE, ORAL CAVITY2016-04-04

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