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What is Multiple Listing for UL certified products?
Multiple Listing is the procedure to use the UL Mark on identical UL Certified products under different brand names.
What is the benefit to apply Multiple Listing for UL certified products?
The benefits include:
(1) the right to include your company’s name in UL’s directory.
(2) superior marketability to retailers and others in your supply chain
(3) recognition by consumers that the product has met applicable safety requirements.
(1) the right to include your company’s name in UL’s directory.
(2) superior marketability to retailers and others in your supply chain
(3) recognition by consumers that the product has met applicable safety requirements.
What is UL 62368-1, Ed.3 effective date for Audio/Video, Information & Communication Technology Equipment?
The effective date is January 6, 2023
What is KC62368-1 effective date for Audio/Video, Information & Communication Technology Equipment?
The official Kats of South Korea issued announcement No. 2021-083 on August 27, 2021 and announced the implementation of KC62668-1. IEC 62368-1 3rd Edition (IEC 62368-1:2018) as the standard KC 62368-1 formulated by Korean safety regulations. The existing safety standards KC60065, K60950-1 and K60950-22 will be implemented and abolished by December 31, 2022.
Under what conditions, the power supply brand and type needs to be listed on the RCM certificate?
When the power supply or battery charger provided with specific electronic (ITE, audio, video) equipment belongs to consumables, the terminal product manufacturer and product category need to be listed on the RCM certificate.
What are the demands of the updated version of the German product safety law ProdSG released on July 16, 2021?
The main demand is to echo the EU's requirements for traceability and accountability of imported products. The GS mark certification certificate issued under the ProdGS specification of the product safety law updates the application requirements. GS requires EU registered address or representative. If the manufacturer of GS application case is located outside the EU or cannot provide an address legally registered in the EU for service of summons, the legal representative shall submit the application on behalf of the manufacturer. The legal representative must be located in the EU or have a legal registered address in the EU to provide service of summons.
Does the EU CE have any requirements for the marking of "importer" and "manufacturer" information on the CE mark?
According to the requirements of low voltage directive 2014 / 35 / EU, the name, trademark and address information of the importer and manufacturer shall be marked on the product. If it cannot be marked on the product, it shall be marked on the package or the accompanying instruction document. Ensure that after the product enters the European market, the product can find the corresponding manufacturer and take the responsibility of product safety.
Why Medical Equipment Directive (MDD) is replaced by Medical Devices Regulation (MDR)?
Due to the loose requirements of the previous MDD, manufacturers of Panel PC or medical power adapter used to declare compliance with MDD by IEC60601-1 test report.