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.

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.

Other Europe (non-EU) Countries: 

Belarus, Bosnia & Herzegovina, IcelandMacedonia, Moldova, Norway, Serbia, Switzerland, Turkey, Ukraine

 

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