Medi Soft S A

FDA Filings

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

FDA Registration(s)
Registration Number3003630525
FEI Number3003630525
NameMEDI SOFT SA
Owner & OperatorMEDISOFT S.A.
Contact Address1, PAE de Sorinnes Route de la voie Cuivree
Sorinnes BE-WNA Namur 5503 BE
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address1, PAE DE SORINNES ROUTE DE LA VOIE CUIVREE
DINANT Namur, 5503 BE
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Medi Soft SA
SpiroAir SP-00-022018-07-06
Medi Soft SA
TransAir3 10-SA-03-TA2018-07-06
Medi Soft SA
BodyBox BB-00-032018-07-06
Medi Soft SA
BodyBox BB-00-022018-07-06
Medi Soft SA
BodyBox BB-00-012018-07-06
MEDI SOFT SA [MEDISOFT S.A.]
TransAir22008-04-15
MEDI SOFT SA [MEDISOFT S.A.]
SpiroAir2008-04-15
MEDI SOFT SA [MEDISOFT S.A.]
Body Box2008-04-15

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