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.



ARE YOU INTERESTED IN REGISTRATION IN LIECHTENSTEIN? REQUEST A FREE QUOTE>​
latest news
  • Sep 19 2017
    REGULATORY UPDATE - SPD

    Korea: SPD's CB11 was approved for sale with LICENSALE.COM®. ...

    Read More
  • Sep 6 2017
    REGULATORY UPDATE - SPD

    Philippines: SPD's IVD products CBDOT were approved for sale with LICENSALE.COM®. ...

    Read More
  • Aug 31 2017
    REGULATORY UPDATE - CORTEX

    USA: Cortex's Dental implants and Prosthetic Devices were approved for sale with LICENSALE.COM®...

    Read More
  • Aug 10 2017
    REGULATORY UPDATE - SPD

    Ethiopia: SPD's CB11, CB9 & CBDOT were approved for sale with LICENSALE.COM®. ...

    Read More
  • Aug 8 2017
    REGULATORY UPDATE - XERIDIEM

    Saudi Arabia: Xeridiems' Entuit family was approved for sale with LICENSALE.COM®. ...

    Read More

VANCOUVER OFFICE

  • Phone +1 604.681.6888
  • Fax +1 604.681.6822
  • info@arazygroup.com
  •  
  • #350-1333 Johnston Street
  • Pier 32, Granville Island
  • Vancouver, British Columbia
  • Canada V6H 3R9

BACK TO TOP