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        Fascia gun EU CE certification——ZRLK

        Author:中認(rèn)聯(lián)科 time:2022-01-24 Ctr:1686

        The fascia gun, also known as the deep myofascial impact instrument, is a soft tissue rehabilitation tool. It relaxes the soft tissues of the body through high-frequency impact, and can relax the muscles after exercise, so as to relieve pain and promote muscle blood circulation. , it is more suitable for people who sit for too long every day or face the computer for a long time, such as office workers, gamers, etc. However, if such products want to export into the EU market, they need to apply for CE certification.

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        The importance of applying for CE certification

        1. Obtaining the CE certification certificate from the designated agency of the European Union can maximize the trust of consumers and market supervision agencies;

        2. In the case of litigation, the CE certification certificate of the EU designated agency will become technical evidence with legal effect;

        3. It can effectively avoid three major risks: (1) the risk of being detained and investigated by the customs; (2) the risk of being investigated and punished by the market supervision agency; (3) the risk of being accused by peers for competition purposes.

        Technical documents required for CE certification application

        1. Product instruction manual

        2. Safety design documents (including key structural drawings, that is, design drawings that can reflect the climbing distance, clearance, number of insulating layers and thickness)

        3. Product technical conditions (or enterprise standards)

        4. Product electrical schematic

        5. Product circuit diagram

        6. List of key components or raw materials (please choose products with European certification marks)

        7. A copy of the certificate of the whole machine or components

        8. Other required information

        Fascia device EU CE certification process

        1. Application acceptance;

        2. Data review;

        3. Receive the samples sent;

        4. Sample test;

        5. Conformity assessment;

        6. Approval;

        7. Printing, receiving, sending and management of reports.

        image.png

        Please contact our company ZRLK for the EU CE certification of the fascia device. We will provide you with professional and efficient testing and certification services with favorable prices and considerate service. If you provide us with product pictures and specifications, we will give corresponding cycles, quotations and specific solutions according to your products. You are welcome to inquire!

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