Cardio Life Research, S.A.
Country not established
- Devices
- 2
What Cardio Life Research, S.A. makes
Cardio Life Research, S.A. manufactures vascular access devices, including the Portaclamp and Portaclamp Flex, which are designed for securing and stabilizing vascular lines in medical procedures.
These products are classified as Class II devices under FDA regulations and are listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Portaclamp Flex Ref K070380
Regimes: 510(k) Registry: 510(k)Portaclamp Ref K033085
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cardio Life Research, S.A. have in the registry?
The registry currently lists 2 devices for Cardio Life Research, S.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cardio Life Research, S.A.'s devices?
Among its 2 most recently registered devices, Cardio Life Research, S.A. has devices listed in FDA 510(k) (2 devices).
What risk classes do Cardio Life Research, S.A.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Cardio Life Research, S.A.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cardio Life Research, S.A. in the registry?
The most recently registered devices listed for Cardio Life Research, S.A. include PORTACLAMP FLEX and PORTACLAMP.