Release time:
2018
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03
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12
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What does ROHS meanRoHS is a mandatory standard established by EU legislation, and its full name is the Directive on Restricting the Use of Certain Hazardous Components in Electronic and Electrical Equipment. The original directive 2002/95/EC was implemented on July 1, 2006, covering eight categories of electronic and electrical equipment (EEEs) with direct current of 1500V and alternating current of 1000V or less. The directive stipulates that the content of lead (Pb), mercury (Hg), hexavalent chromium (Cr (VI)), polybrominated biphenyls (PBBs), and polybrominated biphenyl ethers (PBDEs) in n...
Release time:
2018
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03
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09
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Many enterprises may have doubts when applying for CE certification, such as: What is the purpose of applying for CE certification? What is the validity period of the CE certificate? CE certification process? What materials should be prepared for CE certification?1、 What is the purpose of applying for CE certification?Answer: The advantage of applying for CE certification and affixing the CE certification mark is that CE certification is a free pass to enter the European market. Products with CE certification will greatly increase consumers' trust, as affixing the CE certification mark rep...
Release time:
2018
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03
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08
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On June 4, 2015, the Official Journal of the European Union (OJ) issued RoHS2.0 Revised Directive (EU) 2015/863, officially including DEHP, BBP, DBP, and DIBP in the list of restricted substances in Appendix II. As of now, there are ten mandatory controlled substances in Appendix II. Please refer to the table below for details:Restricted substance limit (mass fraction)Lead (Pb) 0.1%Mercury (Hg) 0.1%Cadmium (Cd) 0.01%Hexavalent chromium (Cr VI) 0.1%Polybrominated biphenyls (PBB) 0.1%Polybrominated diphenyl ethers (PBDE) 0.1%Di (2-ethylhexyl) phthalate (DEHP) 0.1%Tolylbutyl phthalate (BBP) 0.1%D...
Release time:
2018
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03
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07
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What is the EU REACH regulation registration?The registration, evaluation, authorization, and restriction of chemicals regulation (hereinafter referred to as the REACH regulation), which was implemented by the European Union on June 1, 2008, is the primary obligation under this regulation. After successfully submitting a chemical substance registration dossier to the European Chemical Administration (ECHA), enterprises can obtain an 18 digit registration number. Enterprises that fail to complete registration before the corresponding deadline cannot continue to market their corresponding produc...
Release time:
2018
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02
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24
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Which food companies need to apply for FDA certification?Owners, operators, responsible agents, or authorized individuals of domestic or foreign facilities that produce/process, package, or store human food or animal feed for consumption in the United States must certify their facilities to the FDA.Foods that require certification:Alcohol, flour sugar products, beverages, sweets, cereals, cheese, chocolate or cocoa, coffee or tea, food pigments, regular diet or meal alternatives, including pharmaceutical food, functional food (including Chinese herbal medicine), condiments, aquatic products, f...
Release time:
2018
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02
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23
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The food grade FDA certification process includes two parts: registration and testing of relevant standards.FDA certification process for food contact materials:Step 1: Register on the FDA websitePart 2: Testing in accredited third-party laboratories in accordance with FDA food grade standardsThe common FDA certification testing items for materials in contact with food are as follows:Organic coatings, metal, and electroplated products require U.S. FDA CFR 21 175.300Water extractions deionized water extraction method8% alcohol extractionsN-heptane extractions1. Paper Products Requirements U.S. ...
Release time:
2018
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02
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06
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MDD application process The European Union divides medical machinery products into four categories, namely Class I, Class IIa, Class IIb, and Class III. Class I products need to be labeled with the CE mark and can be self declared. That is, the manufacturer prepares technical documentation files for the product, and at the same time tests the product according to relevant EN standards or entrusts a capable laboratory to test and pass the test. If Class IIa, IIb, and III products need to be labeled with the CE mark, they must be verified by a verification agency designated by the Eu...
Release time:
2018
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02
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05
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To successfully pass CE certification for medical device products, three aspects of work need to be done well.Firstly, collect EU technical regulations and EU (EN) standards related to certified products, and digest, absorb, and incorporate them into enterprise product standards.Secondly, the enterprise strictly organizes production in accordance with the above product standards, which means implementing the requirements of the technical regulations and EN standards into the entire process of product design, development, and production manufacturing.Thirdly, enterprises must establish and main...
Release time:
2018
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02
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02
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What does RoHS mean On February 13, 2003, the European Parliament and the European Commission issued the 'Waste Electronic and Electrical Equipment Directive' (referred to as the 'WEEE Directive') and the 'Restriction of the Use of Certain Hazardous Substances in Electronic and Electrical Equipment Directive' (referred to as the 'RoHS Directive') in their official gazettes. 《RoHS Directive》gentle《weee directive》There are 102 types of products in ten major categories that are regulated to be included in the management of hazardous...
Release time:
2018
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01
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26
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一、Fill out the Bede REACH application form1. The handwriting should be clear, such as the number 0 and the English letter O, the number 5 and the English letter S, the number 1 and the English letter I, the number 9 and the English letter P, and the number 2 and the English letter Z should be clearly marked.2. Clearly fill in the testing requirements and indicate the standards or testing methods used as much as possible3. Clear selection of service nature; Working days are the time for verbal notification of results, excluding holidays, sample delivery, receipt, report printing, and mailing.4....