EAC Certification for Russia and the Eurasian Economic Union (TR CU 032/2013): Mandatory Customs Union Declaration of Conformity and Certificate for Pressure Equipment

 EAC Certification for Russia and the Eurasian Economic Union (TR CU 032/2013): Mandatory Customs Union Declaration of Conformity and Certificate for Pressure Equipment



In the unified market of the Eurasian Economic Union, the safety access of pressure equipment is strictly governed by technical regulation TR CU 032/2013. This regulation establishes mandatory safety requirements for the circulation, installation, and operation of pressure equipment within the Union, aiming to protect the safety of human life and health, property, and the environment. For manufacturers and exporters, understanding and completing EAC conformity assessment is a crucial legal step for entering the markets of member states such as Russia, Kazakhstan, and Belarus.


Depending on the risk level and intended use of the equipment, TR CU 032/2013 specifies two main forms of conformity assessment: the EAC Declaration of Conformity and the EAC Certificate of Conformity. The EAC Declaration of Conformity is typically applicable to relatively low-risk pressure equipment. It is a self-declaration by the applicant, based on their own evidence or a test report jointly completed with a certification body, within the Union's unified registration system, that their product complies with regulatory requirements. This is a confirmation model where the applicant assumes primary responsibility. For high-risk equipment, such as critical equipment used under extremely high pressure, high temperature, or involving hazardous media, regulations mandate a comprehensive audit and testing by a certification body to obtain a more authoritative EAC certificate of conformity. Both types of certificates have equal legal effect and are necessary documents for product clearance and sale.


The core process of applying for an EAC declaration of conformity or certificate begins with the preparation of technical documentation. Applicants must prepare detailed product technical documentation, design drawings, safety assessments, bills of materials, and operation manuals. Subsequently, product samples must be sent to an accredited laboratory for mandatory safety testing to ensure compliance with all parameter requirements of TR CU 032/2013 regarding strength, sealing, and safety devices. Based on the test reports and other documents, the certification body conducts an audit and, upon approval, registers the EAC declaration of conformity or issues an EAC certificate of conformity. After successful registration or issuance, the applicant can affix the EAC distribution mark to the product.


It is worth noting that for the serial production of pressure equipment, in addition to obtaining conformity documentation, subsequent production surveillance audits by the certification body may also be required. Failure to obtain the required EAC documentation or illegally affixing EAC markings to products will result in products being refused entry, being forcibly removed from shelves, fines, and even criminal prosecution. Therefore, relevant companies must clearly define the customs codes and risk classifications of their products in advance, select the correct conformity assessment scheme, and ensure the completeness and compliance of their technical documentation in order to efficiently and legally develop the important market of the Eurasian Economic Union.

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