Brosmed Medical B V

FDA Filings

This page includes the latest FDA filings for Brosmed Medical B V. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3014895346
FEI Number3014895346
NameDavid Lennarz
Owner & OperatorBrosMed Medical B.V.
Contact AddressMgr. Buckxstraat 8
Sittard NL-LI Limburg NL-6134 AP NL
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address144 Research Drive
Hampton, VA 23666 US
Establishment TypeExport Device to the United States But Perform No Other Operation on Device



FDA Filings

Device
Company
DeviceDate
David Lennarz [BrosMed Medical B.V.]
Castor, Achilles, and Hermes NC PTA Balloon Dilatation Catheters2019-02-19
David Lennarz [BrosMed Medical B.V.]
Polux, Minerva, and Atropos PTA Balloon Dilatation Catheters2019-02-19
David Lennarz [BrosMed Medical B.V.]
Apollo Balloon Dilatation Catheter2019-02-19
David Lennarz [BrosMed Medical B.V.]
Apollo Balloon Dilatation Catheter2019-02-19
David Lennarz [BrosMed Medical B.V.]
Artimes Balloon Dilatation Catheter2019-01-30

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