Medical devices in Liechtenstein are regulated by Amt für Gesundheit. Devices that have a CE Mark do not require additional registration.
Devices are classified according to the EU model of risk-based Classes I, IIa, IIb, III and IV. TIMEFRAME:
The EU registration process takes about 4-6 weeks after submission for Class I devices. For the other classes, it depends on the contract with the notified body and the type of device.
Devices can remain on the market as long as their CE Mark is valid. AUTHORIZED REPRESENTATIVE:
An EU authorized representative is required. ADDITIONAL INFORMATION:
All product information must be translated into German.
Last updated on March 17 2015.
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