Angioslide, Ltd.
Country not established
- Devices
- 20
What Angioslide, Ltd. makes
Angioslide, Ltd. manufactures peripheral angioplasty balloon catheters designed for the dilation of narrowed or blocked arteries in the peripheral vascular system. The PROTEUS device is intended for use in interventional procedures to restore blood flow in lower limb arteries.
The PROTEUS peripheral angioplasty balloon catheter is classified as a Class II medical device under FDA regulations. It is listed in the FDA’s 510(k) and UDI databases, reflecting its authorised status for commercial distribution in the United States.
Catalogue
Search and filter all 20 devicesCompany details
- DUNS number
- 514451397
- [email protected]
- Phone
- +972523265853
Frequently asked questions
How many devices does Angioslide, Ltd. have in the registry?
The registry currently lists 20 devices for Angioslide, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Angioslide, Ltd.'s devices?
Among its 20 most recently registered devices, Angioslide, Ltd. has devices listed in FDA 510(k) (6 devices) and FDA GUDID (14 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Angioslide, Ltd.'s devices fall under?
Among its 20 most recently registered devices, the classes recorded for Angioslide, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Angioslide, Ltd. in the registry?
The most recently registered devices listed for Angioslide, Ltd. include PROTEUS 1U-0640-135-02, PROTEUS 1U-0560-135-03, PROTEUS 1U-0660-135-03 and PROTEUS 1U-0520-135-02.