Andi Electromedical Aps
Country not established
- Devices
- 1
What Andi Electromedical Aps makes
Andi Electromedical Aps manufactures the POWER LASER 90, a medical laser device designed for specific clinical applications.
The POWER LASER 90 is classified as a Class II device and is listed under the FDA’s 510(k) pathway. The company is based in the US.
Catalogue
Power Laser 90 Ref K030692
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Andi Electromedical Aps have in the registry?
The registry currently lists 1 device for Andi Electromedical Aps. Devices recorded under merged duplicate company entries are counted once.
Which registries list Andi Electromedical Aps's devices?
Among its 1 most recently registered device, Andi Electromedical Aps has devices listed in FDA 510(k) (1 device).
What risk classes do Andi Electromedical Aps's devices fall under?
Among its 1 most recently registered device, the classes recorded for Andi Electromedical Aps's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Andi Electromedical Aps in the registry?
The most recently registered devices listed for Andi Electromedical Aps include POWER LASER 90.