# ABIOMED EUROPE GMBH

FEI: 3007904765
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: Abiomed Europe GmbH (#10030761)

Address: Neuenhofer Weg 3, Aachen North Rhine-Westphalia, 52074, DE

Mandatory US Agent: Abiomed, Inc.

## Products

Total registered: 1
Top product codes: PYX
Regulation §: 870.4360

Proprietary names: Impella RP, Impella RP Flex with SmartAssist, Impella RP with SmartAssist

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223007904765%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3007904765