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RECK-Technik GmbH & Co. KG

Active in EUDAMED

Germanyfrom SRN EUDAMED FDA SRN DE-MF-000005730 FEI 3004704224

Devices
30
Registrations
EUDAMEDFDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

European Union
EUDAMED actor
United States
FDA FEI

Catalogue30

Newest first, rows 1-30 of 30

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  • MOTOmed layson Ref 261.230

    Class IIa
    Active CE MDR EUDAMED IIa
  • MOTOmed loop Ref 260.038

    Class IIa
    Active CE MDR EUDAMED IIa
  • MOTOmed muvi Ref 300.008

    Class IIa
    Active CE MDR EUDAMED IIa
  • MOTOmed loop Ref 260.070

    Class IIa
    Active CE MDR EUDAMED IIa
  • MOTOmed loop Ref 260.080

    Class IIa
    Active CE MDR EUDAMED IIa
  • MOTOmed loop Ref 260.030

    Class IIa
    Active CE MDR EUDAMED IIa
  • MOTOmed muvi Ref 300.220

    Class IIa
    Active CE MDR EUDAMED IIa
  • MOTOmed loop Ref 260.600

    Class IIa
    Active CE MDR EUDAMED IIa
  • MOTOmed loop Ref 260.020

    Class IIa
    Active CE MDR EUDAMED IIa
  • MOTOmed loop Ref 260.090

    Class IIa
    Active CE MDR EUDAMED IIa
  • MOTOmed layson Ref 261.010

    Class IIa
    Active CE MDR EUDAMED IIa
  • MOTOmed layson Ref 261.330

    Class IIa
    Active CE MDR EUDAMED IIa
  • MOTOmed loop Ref 260.120

    Class IIa
    Active CE MDR EUDAMED IIa
  • MOTOmed gracile Ref 263.010

    Class IIa
    Active CE MDR EUDAMED IIa
  • MOTOmed gracile Ref 263.030

    Class IIa
    Active CE MDR EUDAMED IIa
  • MOTOmed layson Ref 261.310

    Class IIa
    Active CE MDR EUDAMED IIa
  • MOTOmed layson Ref 261.210

    Class IIa
    Active CE MDR EUDAMED IIa
  • MOTOmed layson Ref 261.110

    Class IIa
    Active CE MDR EUDAMED IIa
  • MOTOmed layson Ref 261.600

    Class IIa
    Active CE MDR EUDAMED IIa
  • MOTOmed loop Ref 260.100

    Class IIa
    Active CE MDR EUDAMED IIa
  • MOTOmed muvi Ref 300.000

    Class IIa
    Active CE MDR EUDAMED IIa
  • MOTOmed layson Ref 261.139

    Class IIa
    Active CE MDR EUDAMED IIa
  • MOTOmed layson Ref 261.030

    Class IIa
    Active CE MDR EUDAMED IIa
  • MOTOmed loop Ref 260.060

    Class IIa
    Active CE MDR EUDAMED IIa
  • MOTOmed loop Ref 260.040

    Class IIa
    Active CE MDR EUDAMED IIa
  • MOTOmed loop Ref 260.010

    Class IIa
    Active CE MDR EUDAMED IIa
  • MOTOmed loop Ref 260.110

    Class IIa
    Active CE MDR EUDAMED IIa
  • MOTOmed layson Ref 261.130

    Class IIa
    Active CE MDR EUDAMED IIa
  • MOTOmed loop Ref 260.039

    Class IIa
    Active CE MDR EUDAMED IIa
  • MOTOmed layson Ref 261.119

    Class IIa
    Active CE MDR EUDAMED IIa

Rows 1-30 of 30

Company details

EUDAMED SRN
DE-MF-000005730
FDA FEI number
3004704224
EU VAT number
DE812038881
EUDAMED status
Active
EUDAMED registered name
RECK-Technik GmbH & Co. KG
EUDAMED abbreviated name
RECK-Technik GmbH & Co. KG
Registered address
1-5, Reckstraße, 88422, Betzenweiler, Germany
Phone
+4973741884(from company website)
PRRC contact
Andreas Brauch(public in EUDAMED)

From the company website

Read 18 Sep 2026

MOTOmed – the most used motor-powered movement therapy device. Suitable for people with spasticity and movement restrictions as well as wheelchair users.

Translated from the manufacturer's own website. Source

Frequently asked questions

How many devices does RECK-Technik GmbH & Co. KG have in the registry?

The registry currently lists 30 devices for RECK-Technik GmbH & Co. KG. Devices recorded under merged duplicate company entries are counted once.

Which registries list RECK-Technik GmbH & Co. KG's devices?

Among its 30 most recently registered devices, RECK-Technik GmbH & Co. KG has devices listed in EUDAMED (30 devices).

What risk classes do RECK-Technik GmbH & Co. KG's devices fall under?

Among its 30 most recently registered devices, the classes recorded for RECK-Technik GmbH & Co. KG's devices are Class IIa. Each device page shows its own class and authorisation.

What are the newest devices from RECK-Technik GmbH & Co. KG in the registry?

The most recently registered devices listed for RECK-Technik GmbH & Co. KG include MOTOmed layson, MOTOmed loop, MOTOmed muvi and MOTOmed gracile.

Generated automatically from registry data and not verified by a human reviewer.