Cardiogard Medical, Ltd.
Country not established
- Devices
- 3
What Cardiogard Medical, Ltd. makes
Cardiogard Medical, Ltd. makes cardiopulmonary bypass and extracorporeal membrane oxygenation cannulae, specifically return cannulae, such as the CardioGard Emboli Protection Cannula. These devices are used in medical procedures to protect against emboli. The company's products are focused on cardiopulmonary bypass and related applications.
The company's portfolio is regulated as Class II devices and is listed in the FDA's 510(k) and UDI registries. Cardiogard Medical, Ltd. is based in the US. The devices are subject to regulatory oversight by the FDA.
Catalogue
- Registry: GUDID
CardioGard Emboli Protection Cannula Ref K182302
Regimes: 510(k) Registry: 510(k)Cardiogard Emboli Protection Cannula Ref K141465
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 533658675
Frequently asked questions
How many devices does Cardiogard Medical, Ltd. have in the registry?
The registry currently lists 3 devices for Cardiogard Medical, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cardiogard Medical, Ltd.'s devices?
Among its 3 most recently registered devices, Cardiogard Medical, Ltd. has devices listed in FDA 510(k) (2 devices) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Cardiogard Medical, Ltd.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Cardiogard Medical, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cardiogard Medical, Ltd. in the registry?
The most recently registered devices listed for Cardiogard Medical, Ltd. include CardioGard Emboli Protection Cannula CGT2422 and CardioGard Emboli Protection Cannula.