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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.
Last updated on November 24th, 2021.
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.
Other Europe (non-EU) Countries: Belarus, Bosnia & Herzegovina, Iceland, Macedonia, Moldova, Norway, Serbia, Switzerland, Turkey, Ukraine
For detailed device-specific compliance information for each market, including Liechtenstein, to expedite the preparation of your medical device or IVD registration application.
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