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.
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