Liechtenstein Medical Device Registration

Medical Device Oversight in Liechtenstein: AG Regulations and Compliance

Regulatory Authority

Amt für Gesundheit – Office of Public Health (AG)

The Office of Public Health (AG) works to serve the entire population of Liechtenstein. Our customers are also service providers in the healthcare sector, communities, schools, commissions, other offices, institutions, companies, etc.

Link for Regulatory Authority

https://www.llv.li/inhalt/1908/amtsstellen/amt-fur-gesundheit

Classification of Medical Devices

• Class I
• Class IIa
• Class IIb
• Class III
• Class IV

Registration Timeline

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 for Liechtenstein Medical Device Registration

Devices can remain on the market as long as their CE Mark is valid.

Special Labelling Requirements

All product information must be translated into German

Who should make this Communication?

• Manufacturer
• Authorized Representative

When to make this Communication?

Before placing a medical device into the market.

How OMC Medical can assist you with the process?

• Act as your Authorized representative

Why Choose Us?

• Working towards client satisfaction
• Cost effective solutions
• Project completion before deadline
• Quality Regulatory affairs solutions

Contact us for free consultation: sales@omcmedical.com