Technimed, Inc.
Country not established
Part of Technimed AG
- Devices
- 1
What Technimed, Inc. makes
Technimed, Inc. manufactures the Dimension Whole Blood Cholesterol device, a point-of-care analyzer designed for measuring total cholesterol levels in whole blood samples. This device is intended for use in clinical settings to provide rapid, accurate results for patient monitoring and diagnostic purposes.
The Dimension Whole Blood Cholesterol device is classified as a Class I medical device under FDA regulations and is listed via the 510(k) clearance process. The company is based in the United States.
Catalogue
Dimension Whole Blood Cholesterol Ref K880723
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Technimed, Inc. have in the registry?
The registry currently lists 1 device for Technimed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Technimed, Inc.'s devices?
Among its 1 most recently registered device, Technimed, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Technimed, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Technimed, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Technimed, Inc. in the registry?
The most recently registered devices listed for Technimed, Inc. include DIMENSION WHOLE BLOOD CHOLESTEROL.