Dipro Diagnostic Products GmbH
Country not established
- Devices
- 1
What Dipro Diagnostic Products GmbH makes
Dipro Diagnostic Products GmbH manufactures the HEMDETECT test, a diagnostic device designed to detect occult blood in fecal samples for medical screening purposes.
The HEMDETECT test is classified as a Class II medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Hemdetect(R) Test For Occult Blood In Feces Ref K936056
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dipro Diagnostic Products GmbH have in the registry?
The registry currently lists 1 device for Dipro Diagnostic Products GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dipro Diagnostic Products GmbH's devices?
Among its 1 most recently registered device, Dipro Diagnostic Products GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Dipro Diagnostic Products GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Dipro Diagnostic Products GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dipro Diagnostic Products GmbH in the registry?
The most recently registered devices listed for Dipro Diagnostic Products GmbH include HEMDETECT(R) TEST FOR OCCULT BLOOD IN FECES.