Medikomp G M B H

FDA Filings

This page includes the latest FDA filings for Medikomp 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 Number3007427881
FEI Number3007427881
NameMEDIKOMP GMBH
Owner & OperatorMediKomp GmbH
Contact AddressKEHLER STRASSE 31
Rastatt DE-BW Baden-Wurttemberg 76437 DE
Official Correspondent
  • Marc Zimmermann
  • 49-722-29321487-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressKehler Strasse 31
Rastatt Baden-Wurttemberg, 76437 DE
Establishment TypeManufacture Medical Device for Another Party (Contract Manufacturer)



FDA Filings

Device
Company
DeviceDate
MEDIKOMP GMBH
ROTAFLOW Emergency Drive2012-08-22
MEDIKOMP GMBH
ROTAFLOW Drive Unit2012-08-22
MEDIKOMP GMBH
ROTAFLOW Console2012-08-22
MEDIKOMP GMBH
Heart Lung Machine HL-20 Twin Pump2012-08-22
MEDIKOMP GMBH
Heart Lung Machine HL-202012-08-22
MEDIKOMP GMBH
CARDIOHELP-i, CARDIOHELP Emergency Drive, Accessories2012-08-22
MEDIKOMP GMBH
SPRINTER CART, SPRINTER CART XL2012-08-22
MEDIKOMP GMBH
VAVD Controller2012-08-22

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