Hei, Inc.
Country not established
- Devices
- 1
What Hei, Inc. makes
Hei, Inc. manufactures the HEITER 3000 Hyperthermic Perfusion System, a device designed for localized hyperthermia therapy to treat specific medical conditions through controlled tissue heating.
The company’s portfolio is regulated under FDA Class II devices, with the HEITER 3000 Hyperthermic Perfusion System listed via a 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Heiter 3000 Hyperthermic Perfusion System Ref K102900
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hei, Inc. have in the registry?
The registry currently lists 1 device for Hei, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hei, Inc.'s devices?
Among its 1 most recently registered device, Hei, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Hei, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Hei, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hei, Inc. in the registry?
The most recently registered devices listed for Hei, Inc. include HEITER 3000 HYPERTHERMIC PERFUSION SYSTEM.