Metronic Electronic GmbH
Country not established
- Devices
- 1
What Metronic Electronic GmbH makes
Metronic Electronic GmbH manufactures external automated external defibrillators (AEDs) under the PRIMEDIC brand, designed for emergency cardiac resuscitation to restore normal heart rhythms in patients experiencing sudden cardiac arrest.
The company’s defibrillators are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The portfolio is regulated in the United States, where the manufacturer is based.
Catalogue
Primedic Defibrillators-N/B Ref K921765
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Metronic Electronic GmbH have in the registry?
The registry currently lists 1 device for Metronic Electronic GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Metronic Electronic GmbH's devices?
Among its 1 most recently registered device, Metronic Electronic GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Metronic Electronic GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Metronic Electronic GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Metronic Electronic GmbH in the registry?
The most recently registered devices listed for Metronic Electronic GmbH include PRIMEDIC DEFIBRILLATORS-N/B.