Reminder Ce Marking And Declaration Responsibilities

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Reminder Marking Declaration Responsibilities
  • Guatemalan Customs Declaration for 8-Figure Fiber Optic Cable ADSS

    Guatemalan Customs Declaration for 8-Figure Fiber Optic Cable ADSS

    The Division of Registration and Control of Medicines and Foods of the Ministry of Health issues import permits for medical devices, pharmaceutical products, and cosmetics. Some products require an inscrip.


  • New Circulating Light Device with CE Certification

    New Circulating Light Device with CE Certification

    -- (BUSINESS WIRE)--Cerus Corporation (Nasdaq: CERS) announced today the CE mark approval of its next-generation LED-based illumination device, or the INT200, for the INTERCEPT Blood System for platelets and plasma under the European Union (EU) Medical Device. CONCORD, Calif. Such EU directives and regulations apply to a wide range of products, including electronics, toys, helmets, sunglasses, and medical devices. With this marking, the manufacturer indicates that a product meets the requirements set out in EU product rules. For lighting products, CE certification indicates compliance with the basic requirements of relevant EU directives on safety, health, and environmental protection. European Norms Electrical Certification, or ENEC for short, regulates the certification of luminaires, office equipment and components such as switches and cables. For LED products, this typically includes the Low Voltage Directive (LVD) 2014/35/EU, the.

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