Biosys Biyomedikal Muhendislik San. VE Tic. A.S.
TürkiyeFDA applicant, unverified
- Devices
- 1
What Biosys Biyomedikal Muhendislik San. VE Tic. A.S. makes
Biosys Biyomedikal Muhendislik San. VE Tic. A.S. manufactures the Bioscope Neuromonitor Device, a medical instrument designed for real-time monitoring of neurological signals during surgical procedures or intensive care settings.
The company’s portfolio is regulated under Class II devices in the US, with the Bioscope Neuromonitor Device listed via the FDA’s 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Bioscope Neuromonitor Device Ref K233001
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Biosys Biyomedikal Muhendislik San. VE Tic. A.S. have in the registry?
The registry currently lists 1 device for Biosys Biyomedikal Muhendislik San. VE Tic. A.S.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biosys Biyomedikal Muhendislik San. VE Tic. A.S.'s devices?
Among its 1 most recently registered device, Biosys Biyomedikal Muhendislik San. VE Tic. A.S. has devices listed in FDA 510(k) (1 device).
What risk classes do Biosys Biyomedikal Muhendislik San. VE Tic. A.S.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Biosys Biyomedikal Muhendislik 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 Biosys Biyomedikal Muhendislik San. VE Tic. A.S. in the registry?
The most recently registered devices listed for Biosys Biyomedikal Muhendislik San. VE Tic. A.S. include Bioscope Neuromonitor Device.