Matia Robotics Mekatroik Sis. Ar-GE Muh. Yaz.San VE Tic.A.S
TürkiyeFDA applicant, unverified
- Devices
- 1
What Matia Robotics Mekatroik Sis. Ar-GE Muh. Yaz.San VE Tic.A.S makes
Matia Robotics Mekatroik Sis. Ar-Ge Muh. Yaz.San VE Tic.A.S makes the Tek RMD (Tek Robotic Mobilization Device), a robotic mobilization device designed to assist with patient movement and mobility support.
The Tek RMD is classified as a Class II medical device and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Tek RMD (Tek Robotic Mobilization Device) Ref K150548
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Matia Robotics Mekatroik Sis. Ar-Ge Muh. Yaz.San VE Tic.A.S have in the registry?
The registry currently lists 1 device for Matia Robotics Mekatroik Sis. Ar-Ge Muh. Yaz.San VE Tic.A.S. Devices recorded under merged duplicate company entries are counted once.
Which registries list Matia Robotics Mekatroik Sis. Ar-Ge Muh. Yaz.San VE Tic.A.S's devices?
Among its 1 most recently registered device, Matia Robotics Mekatroik Sis. Ar-Ge Muh. Yaz.San VE Tic.A.S has devices listed in FDA 510(k) (1 device).
What risk classes do Matia Robotics Mekatroik Sis. Ar-Ge Muh. Yaz.San VE Tic.A.S's devices fall under?
Among its 1 most recently registered device, the classes recorded for Matia Robotics Mekatroik Sis. Ar-Ge Muh. Yaz.San VE Tic.A.S's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Matia Robotics Mekatroik Sis. Ar-Ge Muh. Yaz.San VE Tic.A.S in the registry?
The most recently registered devices listed for Matia Robotics Mekatroik Sis. Ar-Ge Muh. Yaz.San VE Tic.A.S include Tek RMD (Tek Robotic Mobilization Device).