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LifeTech Scientific (Europe) B.V.

Netherlands NL-MF-000005742 Last updated 17 Sep 2026

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Devices
509
Registries
EUDAMED
FDA recalls
0

Catalogue509

Page 1 of 11

  • Cera Ref LE-ASD-06

    Class III EUDAMED Active

  • Cera Ref LE-VSD-Ecc-04

    Class III EUDAMED Active

  • Ankura Ref LE-TAA4444B160

    Class III EUDAMED Active

  • Ankura Ref LE-AAA2210B160

    Class III EUDAMED Active

  • HeartR Ref LEFVM24AII

    Class III EUDAMED Active

  • Ankura Ref LE-TAA2424B080

    Class III EUDAMED Active

  • SteerEase Ref LE-SFP11F-f

    Class IIa EUDAMED Active

  • SteerEase Ref LE-SFP13F-f

    Class IIa EUDAMED Active

  • Ankura Ref LE-TAA2424B100

    Class III EUDAMED Active

  • Fustar Ref LE-SVB8F-550

    Class IIa EUDAMED Active

  • HeartR Ref LEFVM08AII

    Class III EUDAMED Active

  • Cera Ref LE-PLUG-04

    Class III EUDAMED Active

  • Cera Ref LE-PDA-1214

    Class III EUDAMED Active

  • SteerEase Ref LE-SFA10F

    Class IIa EUDAMED Active

  • SeQure Ref LE-SG-10

    Class IIa EUDAMED Active

  • CeraFlex Ref LE-PDAf-2022

    Class III EUDAMED Active

  • CeraFlex Ref LE-ASDf-08

    Class III EUDAMED Active

  • HeartR Ref LEFS4040

    Class III EUDAMED Active

  • Ankura Ref LE-TAA3838B160

    Class III EUDAMED Active

  • Ankura Ref LE-cuff1412C060

    Class III EUDAMED Active

  • Ankura Ref LE-TAA3224B160

    Class III EUDAMED Active

  • Ankura Ref LE-cuff1214C120

    Class III EUDAMED Active

  • CeraFlex Ref LE-ASDf-24

    Class III EUDAMED Active

  • Ankura Ref LE-TAA3022B200

    Class III EUDAMED Active

  • HeartR Ref LEFVJ16

    Class III EUDAMED Active

  • Ankura Ref LE-TAA2020B040

    Class III EUDAMED Active

  • Ankura Ref LE-AAA2010B100

    Class III EUDAMED Active

  • Ankura Ref LE-cuff1214C060

    Class III EUDAMED Active

  • HeartR Ref LEFS16

    Class III EUDAMED Active

  • Ankura Ref LE-TAA3224B140

    Class III EUDAMED Active

  • Ankura Ref LE-cuff1416C040

    Class III EUDAMED Active

  • Ankura Ref LE-cuff1412C100

    Class III EUDAMED Active

  • Cera Ref LE-VSD-MU-18

    Class III EUDAMED Active

  • HeartR Ref LEFS30

    Class III EUDAMED Active

  • Cera Ref LE-VSD-Sym-18

    Class III EUDAMED Active

  • Cera Ref LE-VSD-Sym-08

    Class III EUDAMED Active

  • HeartR Ref LEFS3535

    Class III EUDAMED Active

  • Ankura Ref LE-TAA4032B200

    Class III EUDAMED Active

  • SteerEase Ref LE-SFA9F-f

    Class IIa EUDAMED Active

  • Cera Ref LE-ASD-08

    Class III EUDAMED Active

  • HeartR Ref LEFVJ05

    Class III EUDAMED Active

  • HeartR Ref LEFVM07B

    Class III EUDAMED Active

  • Ankura Ref LE-cuff1618C060

    Class III EUDAMED Active

  • Ankura Ref LE-AAA2412B160

    Class III EUDAMED Active

  • Konar-Mf Ref LE-MFO-10-8

    Class III EUDAMED Active

  • Cera Ref LE-VSD-Sym-16

    Class III EUDAMED Active

  • Ankura Ref LE-TAA3430B180

    Class III EUDAMED Active

  • HeartR Ref LEFVM10B

    Class III EUDAMED Active

  • Ankura Ref LE-cuff1420C060

    Class III EUDAMED Active

  • Ankura Ref LE-cuff1210C040

    Class III EUDAMED Active

Showing 1-50 of 509

What LifeTech Scientific (Europe) B.V. makes

LifeTech Scientific (Europe) B.V. manufactures orthopaedic and cardiovascular medical devices, including spinal fixation systems (such as the Cera and SteerEase), bone growth stimulators (Ankura), and a vascular closure device (Fustar). Their portfolio also includes a cardiac monitoring or diagnostic device (HeartR).

The company’s devices are classified under EU regulations as Class III (high-risk) and Class IIa (moderate-risk), with all products registered in the EU’s eudamed database. LifeTech Scientific (Europe) B.V. is based in the Netherlands.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does LifeTech Scientific (Europe) B.V. manufacture?

LifeTech Scientific (Europe) B.V. specialises in orthopaedic and cardiovascular medical devices. Their portfolio includes spinal fixation systems like the Cera and SteerEase, bone growth stimulators such as Ankura, a vascular closure device called Fustar, and a cardiac monitoring or diagnostic device named HeartR. These devices address critical areas like spinal stability, bone healing, vascular procedures, and cardiac diagnostics.

Where is LifeTech Scientific (Europe) B.V. based?

LifeTech Scientific (Europe) B.V. is headquartered in the Netherlands. The country’s regulatory framework aligns with EU requirements, ensuring compliance for devices marketed within the European Economic Area.

Which regulatory registries list LifeTech Scientific (Europe) B.V.’s devices?

All of LifeTech Scientific (Europe) B.V.’s devices are registered in the EU’s official medical device database, eudamed. This platform is mandated for transparency and traceability under EU Medical Device Regulations (MDR) and In Vitro Diagnostic Regulation (IVDR), ensuring authorised devices are publicly documented.

How are LifeTech Scientific (Europe) B.V.’s devices classified under EU regulations?

LifeTech Scientific (Europe) B.V.’s devices are classified as Class III (high-risk) or Class IIa (moderate-risk) under EU regulations. Class III includes devices like vascular closure systems or certain cardiac diagnostics, which require stringent pre-market approval due to their critical role in patient safety. Class IIa devices, such as some bone growth stimulators, undergo rigorous conformity assessments but carry lower inherent risks.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Netherlands
Address
Spoorlaan Noord 2, 6043AK Roermond, The Netherland, Roermond, Netherlands
PRRC contact
Ling Li
EUDAMED SRN
NL-MF-000005742