NEXACorteX s.r.o.
Active in EUDAMEDCzechiafrom SRN EUDAMED SRN CZ-MF-000053063
- Devices
- 1
- Registrations
- EUDAMED
At a glance
Market reach
- European Union
- EUDAMED actor
What NEXACorteX s.r.o. makes
NEXACorteX s.r.o. manufactures the OptoSense Spectra, a screening device designed for rapid and reliable assessment of visual and auditory function using optotypes. It is intended for use in both pediatric and adult populations to facilitate quick evaluations of eye and hearing health.
The OptoSense Spectra is classified as a Class I medical device and is registered in the EU’s eudamed database. The company is based in the Czech Republic.
Catalogue
OptoSense Spectra Ref OS-SPECTRA-001
Regimes: CE MDR Registry: EUDAMED
Company details
- EUDAMED SRN
- CZ-MF-000053063
- EUDAMED status
- Active
- EUDAMED registered name
- NEXACorteX s.r.o.
- Registered address
- 2569/108, Korunní, 101 00, Praha, Czechia
- Website
- www.optosense.cz
- [email protected]
- Phone
- +420774945803
- PRRC contact
- Stanislav Kukal
From the company website
OptoSense is a screening tool with optotypes for rapid and reliable eye and hearing examination in children and adults.
Frequently asked questions
How many devices does NEXACorteX s.r.o. have in the registry?
The registry currently lists 1 device for NEXACorteX s.r.o.. Devices recorded under merged duplicate company entries are counted once.
Which registries list NEXACorteX s.r.o.'s devices?
Among its 1 most recently registered device, NEXACorteX s.r.o. has devices listed in EUDAMED (1 device).
What risk classes do NEXACorteX s.r.o.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for NEXACorteX s.r.o.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from NEXACorteX s.r.o. in the registry?
The most recently registered devices listed for NEXACorteX s.r.o. include OptoSense Spectra.