Liechtenstein
REGULATORY AUTHORITY: Medical devices in Liechtenstein are regulated by Amt für Gesundheit. Devices that have a CE Mark do not require additional registration.

CLASSIFICATION SYSTEM:
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.

LICENSE VALIDITY:
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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