Techmedic Development International B.V.
NetherlandsFDA applicant, unverified
- Devices
- 1
What Techmedic Development International B.V. makes
Techmedic Development International B.V. manufactures the Dyna-Vision Telemonitoring System, a device designed for remote patient monitoring and telehealth applications. It facilitates real-time data transmission and monitoring of vital signs or clinical parameters, enabling healthcare providers to assess patient status remotely.
The Dyna-Vision Telemonitoring System is classified as a Class II 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
Dyna-Vision Telemonitoring System Ref K152973
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Techmedic Development International B.V. have in the registry?
The registry currently lists 1 device for Techmedic Development International B.V.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Techmedic Development International B.V.'s devices?
Among its 1 most recently registered device, Techmedic Development International B.V. has devices listed in FDA 510(k) (1 device).
What risk classes do Techmedic Development International B.V.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Techmedic Development International B.V.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Techmedic Development International B.V. in the registry?
The most recently registered devices listed for Techmedic Development International B.V. include Dyna-Vision Telemonitoring System.