Abiomed Europe G M B H

FDA Filings

This page includes the latest FDA filings for Abiomed Europe 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 Number3007904765
FEI Number3007904765
NameABIOMED EUROPE GMBH
Owner & OperatorAbiomed Europe GmbH
Contact AddressNeuenhofer Weg 3
Aachen DE-NW Nordrhein-Westfalen 52074 DE
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressNeuenhofer Weg 3
Aachen Nordrhein-Westfalen, 52074 DE
Establishment TypeManufacture Medical Device

FDA Filings

Device
Company
DeviceDate
ABIOMED EUROPE GMBH
Impella LD2018-02-27
ABIOMED EUROPE GMBH
Impella CP2018-02-27
ABIOMED EUROPE GMBH
Impella 5.02018-02-27
ABIOMED EUROPE GMBH
Impella 2.52018-02-27
ABIOMED EUROPE GMBH
Impella RP2017-11-09
ABIOMED EUROPE GMBH
Impella Purge Cassette2012-11-02
ABIOMED EUROPE GMBH
Impella CP2012-11-02

Related Finance Registrations
NCAGE CodeCL748ABIOMED EUROPE GMBH
CAGE CodeCL748ABIOMED EUROPE GMBH
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