Pmp Industries
Country not established
- Devices
- 1
What Pmp Industries makes
Pmp Industries manufactures the HEMO-DE, a device designed for hemodialysis applications, including blood filtration and purification systems used in renal care settings.
The HEMO-DE is classified as a Class I medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Hemo-De Ref K822784
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pmp Industries have in the registry?
The registry currently lists 1 device for Pmp Industries. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pmp Industries's devices?
Among its 1 most recently registered device, Pmp Industries has devices listed in FDA 510(k) (1 device).
What risk classes do Pmp Industries's devices fall under?
Among its 1 most recently registered device, the classes recorded for Pmp Industries's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Pmp Industries in the registry?
The most recently registered devices listed for Pmp Industries include HEMO-DE.