Medical Device Registration and Approval in Liechtenstein

General country-specific regulatory information is provided on this page for medical device registration and approval in Liechtenstein. Become a LICENSALE.COM user to receive detailed device-specific compliance information for each market, including Liechtenstein, to expedite the preparation of your medical device or IVD registration application.

Medical Device Regulations and Classification in Liechtenstein

REGULATORY AUTHORITY: 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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