LifeTech Scientific (Europe) B.V.
NL-MF-000005742 · Netherlands · Roermond
LifeTech Scientific (Europe) B.V. is registered in the European database on medical devices as a manufacturer, with 792 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class I | 685 |
|---|---|
| Class IIa | 107 |
Most frequent device types declared: LE-AAA2010B140, LE-AAA2412B100, LE-AAA2412B130, LE-AAA2412B160, LE-AAA2612B130.
Among these devices, 791 are declared sterile, 687 implantable.
Devices declared under this manufacturer
- Ankura
- Cera
- CeraFlex
- Fustar
- HeartR
- KONAR-MF
- P070401020102
- SeQure
- SteerEase
Showing 12 of 792 declared devices.
Catalogue references include LE-ASDf-12, LE-TAA2828B120, LE-VSD-Asym-22, LE-VSD-Sym-12, LE-cuff1214C120, LE-cuff1414C040.
European nomenclature codes declared: P070401020102, P07040301, P070401020101, P0780, P07040302, P0704010202.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 792 |
| Country of registration | Netherlands |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 792 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. LifeTech Scientific (Europe) B.V. was not found in either the U.S. or the Canadian register.