Dideco
Country not established
- Devices
- 5
What Dideco makes
Dideco manufactures medical devices for perfusion and extracorporeal circulation, including autotransfusion systems, vacuum pumps, and hollow fiber oxygenators with optional venous reservoirs. Their portfolio also includes perfusion monitoring systems designed for critical care applications, such as tracking fluid dynamics during surgical procedures.
The company’s devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. Their products are based in the United States.
Catalogue
Dideco Compact-A Autotransfusion System Ref K940519
Regimes: 510(k) Registry: 510(k)Data Master Perfusion Monitoring System Ref K001388
Regimes: 510(k) Registry: 510(k)Dideco Vacuum Pump Ref K936220
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Monolyth Mimesys Hollow Fiber Oxygenator Ref K004001
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dideco have in the registry?
The registry currently lists 5 devices for Dideco. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dideco's devices?
Among its 5 most recently registered devices, Dideco has devices listed in FDA 510(k) (5 devices).
What risk classes do Dideco's devices fall under?
Among its 5 most recently registered devices, the classes recorded for Dideco's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dideco in the registry?
The most recently registered devices listed for Dideco include DIDECO COMPACT-A AUTOTRANSFUSION SYSTEM, DATA MASTER PERFUSION MONITORING SYSTEM, DIDECO VACUUM PUMP and DIDECO D901 LILLIPUT HOLLOW FIBER OXYGENATOR WITH OR WITHOUT SOFT VENOUS RESERVOIR BAG, WITH BIOCOMPATABLE TREATMENT SUR.