RECK-Technik GmbH & Co. KG
Active in EUDAMEDGermanyfrom SRN EUDAMED FDA SRN DE-MF-000005730 FEI 3004704224
- Devices
- 30
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
Catalogue
Search and filter all 30 devicesCompany 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
- Website
- www.motomed.com
- facebook.com/reckmotomedofficial
- [email protected]
- Phone
- +4973741884
- PRRC contact
- Andreas Brauch
From the company website
MOTOmed – the most used motor-powered movement therapy device. Suitable for people with spasticity and movement restrictions as well as wheelchair users.
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.