Dyn-Bioshaf (2006), Ltd.
Country not established
- Devices
- 1
What Dyn-Bioshaf (2006), Ltd. makes
Dyn-Bioshaf (2006), Ltd. manufactures the General Semen Analysis Kit, a diagnostic tool designed for evaluating semen samples in clinical settings. The kit includes components for assessing sperm concentration, motility, and morphology under laboratory conditions.
The company’s product portfolio is regulated as Class II medical devices under FDA guidelines, with the General Semen Analysis Kit authorised through the 510(k) clearance process. The manufacturer is based in the United States.
Catalogue
General Semen Analysis Kit Ref K071737
510(k) 510(k)
Frequently asked questions
How many devices does Dyn-Bioshaf (2006), Ltd. have in the registry?
The registry currently lists 1 device for Dyn-Bioshaf (2006), Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dyn-Bioshaf (2006), Ltd.'s devices?
Among its 1 most recently registered device, Dyn-Bioshaf (2006), Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Dyn-Bioshaf (2006), Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Dyn-Bioshaf (2006), Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dyn-Bioshaf (2006), Ltd. in the registry?
The most recently registered devices listed for Dyn-Bioshaf (2006), Ltd. include GENERAL SEMEN ANALYSIS KIT.