Dideco S.p.A.
Country not established
- Devices
- 22
What Dideco S.p.A. makes
Dideco S.P.A. manufactures extracorporeal membrane oxygenation (ECMO) systems and components, including adult, pediatric, and newborn-infant membrane oxygenators, arterial and venous filters, hemoconcentrators, and centrifugal blood pumps. Their portfolio includes integrated units combining oxygenators with arterial filters and venous reservoirs, as well as standalone devices like hollow fiber oxygenators with specialized coatings and twin reservoirs for ECMO circuits.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The manufacturer is based in the United States and lists its products in the FDA’s 510(k) registry.
Catalogue
Search and filter all 22 devicesFrequently asked questions
How many devices does Dideco S.P.A. have in the registry?
The registry currently lists 22 devices for Dideco S.P.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dideco S.P.A.'s devices?
Among its 22 most recently registered devices, Dideco S.P.A. has devices listed in FDA 510(k) (22 devices).
What risk classes do Dideco S.P.A.'s devices fall under?
Among its 22 most recently registered devices, the classes recorded for Dideco S.P.A.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dideco S.P.A. in the registry?
The most recently registered devices listed for Dideco S.P.A. include DIDECO ELECTA, INTEGRATED UNIT: SYNTHESIS: ADULT MEMBRANE OXYGENATOR WITH INTEGRATED ARTERIAL FILTER AND HARDHSHELL VENOUS/CARDIOTOMY, DHF 0.2 HEMOCONCENTRATOR: DIDECO NEWBORN-INFANT HEMONCENTRATION; DHR 0.6 HEMOCONCENTRATOR: DIDECO PEDIATRIC/SMALL ADULT and IDEAL MIMESYS SYSTEM WITH INTEGRATED VENOUS AIR REMOVAL, CENTRIFUGAL BLOOD PUMP, PUMP BRACKET, ADULT MEMBRANE OXYGENATOR.