The differences between E-mark and e-mark

 The main differences between E-mark and e-mark are as follows:


1. E-mark originates from Regulation No. 10 issued by the ECE; e-mark originates from EU Directives 72/245/EEC, 95/54/EC, and 2004/104/EC.



2. E-mark uses a large "E" in a circular frame, while e-mark uses a small "E" in a rectangular frame.


3. E-mark is applicable globally but is not mandatory; member states can refuse to accept it. e-mark is applicable only to EU member states, and once an e-mark is applied for in one member state, all other member states must recognize the validity of the certificate—mandatory mutual recognition.


4. e-mark mainly applies to complete vehicles. E-mark mainly applies to components.

评论

发表评论

此博客中的热门博文

Power Bank Safety Upgrade: First Mandatory National Standard Issued

图片
 Power Bank Safety Upgrade: First Mandatory National Standard Issued my country's first mandatory national standard, the "Technical Specification for Safety of Power Banks," was published on March 31, 2026, and will officially take effect on April 1, 2027. This standard aims to end long-standing problems in the power bank industry, such as falsely advertised capacity, substandard battery cells, and frequent safety incidents. The new regulation introduces several stringent technical requirements, mandating that battery cells pass a needle penetration test (without catching fire or exploding), and strengthening thermal abuse testing; it also adds tests for whole-device drop and crushing, requires products to be labeled with a safe service life, and improves various protection mechanisms.
阅读全文

EN IEC 62680-1-3/62680-1-2 EU Electronics Standards

图片
To reduce e-waste, the EU is committed to promoting a unified charging technology and interface that supports a variety of electronic products. On November 23, 2022, the EU issued Directive EN IEC 62680-1-3/62680-1-2, requiring electronic product manufacturers to use USB-C charging interface technology in their products. It also requires small and medium-sized portable electronic devices such as mobile phones, tablets, and cameras, as well as laptops, to comply with the USB-C charging interface requirement by 2024 and 2026, respectively. The IEC 62680 testing equipment GRL-USB-PD-C2-EPR, formerly the USB-IF Association's USB PD certification testing instrument, performs PD protocol certification testing. IEC 62680-1-2 and IEC 62680-1-3 incorporate the USB-IF USB PD and Type-C specifications and are currently used for protocol testing and certification corresponding to IEC 62680. IEC 62680-1-2 primarily defines the USB PD power supply specification; IEC 62680-1-3 is a specification ...
阅读全文

What is FDA Certification & What is FDA Registration?

图片
 What is FDA Certification & What is FDA Registration? I. What is the FDA? The FDA, authorized by the U.S. Congress (the federal government), is the highest law enforcement agency specializing in food and drug regulation. Its full name is the Food and Drug Administration. Strictly speaking, there is no such thing as FDA certification; the FDA itself has stated this. Generally, when people talk about FDA certification, they are referring to the following three types: FDA registration, FDA testing, and FDA approval. ① FDA Registration: Companies exporting food, drugs, and medical devices to the United States must register with the FDA, listing their company and products. Otherwise, customs clearance will be denied; this is a mandatory requirement. ② FDA Testing: FDA testing primarily refers to safety testing of food contact materials, testing of product contact packaging, biocompatibility testing of medical products, and clinical safety testing. ③ FDA Approval: This usually appli...
阅读全文