Hako Med G M B H

FDA Filings

This page includes the latest FDA filings for Hako Med 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 Number3007967212
FEI Number3007967212
NameN/A
Owner & OperatorHako-Med Gmbh
Contact AddressStaigstrasse 1
karlsruhe DE-BW Baden-Wurttemberg 76229 DE
Official Correspondent
  • Achim Hansjurgens
  • 49-721-82105533-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressN/A N/A
N/A, NA N/A US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
N/A [Hako-Med Gmbh]
PROElecDT series2010-12-21
N/A [Hako-Med Gmbh]
PROElecDT series2010-12-21
N/A [Hako-Med Gmbh]
ElecDT/VasoPulse series2010-12-21
N/A [Hako-Med Gmbh]
ElecDT/VasoPulse series2010-12-21

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