Medine Dynacor
Country not established
- Devices
- 1
What Medine Dynacor makes
Medine Dynacor manufactures sterile suction catheters designed for medical procedures, incorporating built-in water reservoirs for irrigation during use.
The company’s products fall under FDA Class I devices and are listed via the 510(k) pathway. The portfolio is regulated under US FDA standards, with devices registered in the FDA’s 510(k) clearance database.
Catalogue
Suction Catheter W/Sterile Water Ref K822510
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medine Dynacor have in the registry?
The registry currently lists 1 device for Medine Dynacor. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medine Dynacor's devices?
Among its 1 most recently registered device, Medine Dynacor has devices listed in FDA 510(k) (1 device).
What risk classes do Medine Dynacor's devices fall under?
Among its 1 most recently registered device, the classes recorded for Medine Dynacor's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Medine Dynacor in the registry?
The most recently registered devices listed for Medine Dynacor include SUCTION CATHETER W/STERILE WATER.