Phillips Medisize A S

FDA Filings

This page includes the latest FDA filings for Phillips Medisize A S. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number9710049
FEI Number3003346138
NameMichael van der Woude
Owner & OperatorPhillips-Medisize A/S
Contact AddressGimsinglundvej 20
STRUER DK-82 Region Midtjylland DK-7600 DK
Official Correspondent
  • Claus Bjerg
  • 45-70-301600-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address2500 Bee Cave Road Bldg 1, Suite 300
Austin, TX 78746 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Phillips-Medisize A/S
Skytrofa Auto-Injector 2021-11-01
Phillips-Medisize A/S
myBETAapp 846010632021-10-15
Phillips-Medisize A/S
myBETAapp 846010632021-10-15
Phillips-Medisize A/S
myBETAapp 846010632021-10-15
Phillips-Medisize A/S
myBETAapp 846010632021-10-15
Phillips-Medisize A/S
BETACONNECT 822898012021-10-15
Michael van der Woude [Phillips-Medisize A/S]
Connected Health Platform2018-09-06
Michael van der Woude [Phillips-Medisize A/S]
BETACONNECT Navigator2018-09-06
Michael van der Woude [Phillips-Medisize A/S]
myBETAapp2018-09-06
Michael van der Woude [Phillips-Medisize A/S]
FLEXPRO PENMATE2015-08-19
Michael van der Woude [Phillips-Medisize A/S]
BETACONNECT2015-08-19

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