Product Testing and Certification
Procedure for Certification of Medical Devices in Accordance with the Regulation (EU) 2017/745 on Medical Devices (MDR)
The path for the entry of a medical device to the market starts with an idea and leads through its production and testing to the eventual certification. It is recommended that the manufacturer contact the notified body already at the development s...
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SIQ is a notified body under the new Medical Devices Regulation
The medical device market accounts for more than a quarter of the global market. This is a sector that is constantly and rapidly evolving and requires constant adaptation by all stakeholders. The human population is aging, which is why rehabilitat...
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A successfully completed VCCI (Voluntary Control Council for Interference) registration for MME (multimedia equipment)
In May 2022, SIQ completed the VCCI (Voluntary Control Council for Interference) registration for MME (multimedia equipment). Under the voluntary control measures of the VCCI Council, the members conduct MME (multimedia equipment) testing to verif...
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CENELEC Technical Committee CLC/TC 210 – Electromagnetic Compatibility (EMC)
Technical Committee CLC/TC 210 prepares EMC standards and guidelines with particular emphasis on the application of the EMC Directive and other EU Directives that contain EMC references and coordinates all EMC activities in CENELEC. It brings t...
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Luminaries and ENEC+
SIQ Ljubljana has issued its first ENEC+ certificate for LED luminaires. The products had to pass a safety test first and then more demanding performance tests according to the requirements of PD EPRS 003, including photometry measurements, temper...
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