Idemsa
Country not established
- Devices
- 1
What Idemsa makes
Idemsa manufactures hollow fiber dialyzers designed for hemodialysis procedures, including the Hemophan-based IDEMSA Hemophan Hollow Fiber Dialyzers. These devices are intended for the removal of waste products and excess fluids from the blood of patients with renal failure.
The company’s portfolio is regulated under Class II medical devices in the United States, with relevant products listed via the FDA’s 510(k) pathway. The devices are also subject to compliance with U.S. regulatory standards for hemodialysis equipment.
Catalogue
Idemsa Hemophan Hollow Fiber Dialyzers Ref K991908
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Idemsa have in the registry?
The registry currently lists 1 device for Idemsa. Devices recorded under merged duplicate company entries are counted once.
Which registries list Idemsa's devices?
Among its 1 most recently registered device, Idemsa has devices listed in FDA 510(k) (1 device).
What risk classes do Idemsa's devices fall under?
Among its 1 most recently registered device, the classes recorded for Idemsa's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Idemsa in the registry?
The most recently registered devices listed for Idemsa include IDEMSA HEMOPHAN HOLLOW FIBER DIALYZERS.