ABIOMED EUROPE GMBH
DE Last updated 23 Oct 2026
- Devices
- 0
- Registries
- FDA
- FDA recalls
- 0
Catalogue
No devices listed yet from this manufacturer.
Information
- Country
- DE
- Address
- Neuenhofer Weg 3, Aachen North Rhine-Westphalia
- FDA FEI number
- 3007904765
DE Last updated 23 Oct 2026
No devices listed yet from this manufacturer.