Annette Dusek

FDA Filings

This page includes the latest FDA filings for Annette Dusek. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3007697981
FEI Number3007697981
NameAnnette Dusek
Owner & OperatorMedin Medical Innovations GmbH
Contact AddressAdam-Geisler-Str. 1
Olching DE-BY Bayern 82140 DE
Official Correspondent
  • Heribert Susdorf
  • 49-8142-448460-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address4990 Energy Way
Reno, NV 89502 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Annette Dusek [Medin Medical Innovations GmbH]
Nasal mask for Medijet or Miniflow2010-02-26
Annette Dusek [Medin Medical Innovations GmbH]
Fixation Bonnet for Miniflow2010-02-26
Annette Dusek [Medin Medical Innovations GmbH]
Fixation Bonnet for Medijet2010-02-26
Annette Dusek [Medin Medical Innovations GmbH]
Pediflow2009-03-20
Annette Dusek [Medin Medical Innovations GmbH]
Nuflow (nasa cannula)2009-03-20
Annette Dusek [Medin Medical Innovations GmbH]
Nasal prong for Medijet or Miniflow2009-03-20
Annette Dusek [Medin Medical Innovations GmbH]
Miniflow nCPAP device2009-03-20
Annette Dusek [Medin Medical Innovations GmbH]
Medijet nCPAP Generator2009-03-20

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