YY/T 0310-2025 Pending

YY/T 0310-2025 General specifications for X-ray equipment for computed tomography

This document specifies the composition and requirements of X-ray computed tomography equipment (hereinafter referred to as CT scanning devices), and describes the corresponding test methods.
This document is applicable to CT scanning devices, including those used to provide image data for radiation therapy planning.

Publish Date: 2025-06-18

YY 0300-2025 Pending

YY 0300-2025 Dentistry—Artificial teeth for dental prostheses

This document specifies the classification and requirements for polymer and ceramic teeth used in dental restorations, and describes the corresponding testing methods.
This document is applicable to synthetic resin and ceramic teeth products used in dental restorations.

Publish Date: 2025-06-18

YY 9706.287-2025 Pending

YY 9706.287-2025 Medical electrical equipment—Part 2-87:Particular requirements for basic safety and essential performance of high-frequency ventilators

This document specifies the basic safety and performance requirements for high-frequency ventilators (HFV) used in combination with accessories (hereinafter referred to as "ME devices").
This document applies to patients who may be at risk of life-threatening conditions and require comprehensive care and continuous monitoring in professional medical institutions, operated by professional medical staff. It provides high-frequency ventilation of more than 150 breaths per minute for patients requiring different levels of artificial ventilation support, including those dependent on ventilators.
Note 1: In this document, such environments are referred to as critical care environments. High-frequency ventilators used in such environments are considered life-support devices.
Note 2: In this document, such high-frequency ventilators can provide transport in professional medical institutions (e.g., as a functioning ventilator during transport).
Note 3: High-frequency ventilators used for transport in professional medical institutions are not considered emergency medical service environment ventilators.
Note 4: HFVs are primarily categorized into three types: — High-frequency percussive ventilation (HFPV, typical HFV frequency: 60 breaths per minute to 1,000 breaths per minute); — High-frequency jet ventilation (HFJV, typical HFV frequency: 100 breaths per minute to 1,500 breaths per minute); — High-frequency oscillatory ventilation (HFOV, typical HFV frequency: 180 breaths per minute to 1,200 breaths per minute, typically with an active exhalation phase).
Additionally, HFV nomenclature may be combined or used in conjunction with ventilators operating at a frequency below 150 breaths per minute.
*High-frequency ventilators are not considered physiological closed-loop control systems, unless they use patient physiological variables to adjust ventilation therapy settings.
This document also applies to accesso

Publish Date: 2025-02-26

YY/T 1957-2025 Pending

YY/T 1957-2025 Vacuum washer-disinfectors

This document specifies the performance requirements for negative pressure cleaning and disinfection devices and describes the corresponding test methods.
This document applies to cleaning and disinfection devices that have a negative pressure cleaning function and comply with the applicable provisions of YY/T 0734.1 and the corresponding dedicated standards.
This document does not apply to cleaning and disinfection devices that do not have a negative pressure cleaning function.

Publish Date: 2025-02-26

YY 0459-2025 Pending

YY 0459-2025 Implants for surgery—Acrylic resin cements

This document specifies the physical, mechanical, labeling, and packaging requirements for non-radiopaque and radiopaque curable polymer resin bone cements primarily based on polymethyl methacrylate. These two types of bone cements are intended for use in syringes or in a dough-like state, and are primarily applied for internal fixation of prostheses in artificial joint replacement surgeries. The bone cements are provided in a set of measured sterile powders and sterile liquids, suitable for mixing at the time of implantation.
This document does not address the risks to patients or bone cement users during the use of bone cement.
All requirements and all tests apply only to sterile products.
Note: For other types of bone cements not intended for artificial joint replacement, refer to this document for guidance.

Publish Date: 2025-02-26

YY 0267-2025 Pending

YY 0267-2025 Extracorporeal systems for blood purification—Extracorporeal blood and fluidcircuits for haemodialysers,haemodiafilters,haemofilters and haemoconcentrators

This document specifies the requirements for single-use extracorporeal circulation blood/fluid circuits (hereinafter referred to as extracorporeal circulation blood/fluid circuits) and accessories used in conjunction with blood dialysis, hemodialysis, hemofiltration, and blood concentration, and describes the corresponding test methods.
This document applies to single-use extracorporeal circulation blood/fluid circuits and accessories used in conjunction with blood dialysis, hemodialysis, hemofiltration, and blood concentration.
This document does not apply to: — Hemodialysis machines, hemodialysis filters, or hemofiltration filters; — Plasma separators; — Blood perfusion devices; — Vascular access devices.
Note 1: The requirements for hemodialysis machines, hemodialysis filters, hemofiltration filters, and blood concentrators are specified in YY 0053.
Note 2: The requirements for plasma separators are specified in YY 0465.

Publish Date: 2025-02-26

YY 1105-2024 Pending

YY 1105-2024 Electirc apparatus for gastric lavage

This document specifies the safety and performance requirements for electric gastric lavage machines and describes the corresponding test methods.
This document is applicable to electric gastric lavage machines used for clinical gastric lavage on adult patients in medical institutions.

Publish Date: 2024-09-29

YY 0790-2024 Pending

YY 0790-2024 Hemoperfusion equipment

This document specifies the requirements for blood perfusion equipment and describes the corresponding test methods.
This document applies to the blood perfusion equipment defined in 3.1 (hereinafter referred to as the equipment).
This document does not apply to:
—— Peritoneal dialysis equipment;
—— Centrifugal blood component separation equipment;
—— Continuous blood purification equipment;
—— Plasma exchange equipment;
—— Plasma adsorption equipment;
—— Hemodialysis equipment.

Publish Date: 2024-09-29

YY 0271.2-2024 Pending

YY 0271.2-2024 Dentistry—Water-based cements—Part 2:Resin-modified cements

This document specifies the requirements for resin-modified dental adhesives used for bonding, underlayment or lining, restoration, and fabrication of dental posts and cores, and describes the corresponding test methods. This document applies to resin-modified water-based dental adhesives that are cured through a combination of various reactions, including acid-base reactions and polymerization reactions. For example, traditional polyacrylic acid-based glass ionomer dental adhesives are typically produced by the reaction of an ion-releasing aluminosilicate glass with polyacrylic acid in a water environment. The adhesives covered in this document can typically be cured either through water-based acid-base reactions or polymerization reactions. Note: Manufacturers and testing institutions should pay attention to the closely related international standards ISO 4049 (YY 1042-2023/ISO 4049:2019, MOD) and ISO 9917-1 (YY 0271.1-2016/ISO 9917-1:2007, MOD). When evaluating any specific product, the most suitable of the aforementioned standards should be considered for application.

Publish Date: 2024-09-29

YY 0580-2024 Pending

YY 0580-2024 Cardiovascular implants and artificial organs—Cardiopulmonary bypass systems—Arterial blood line filters

本文件规定了一次性使用无菌动脉管路血液过滤器(以下简称过滤器)的要求,描述了相应的试验方法。
本文件适用于心肺转流手术用过滤器,不适用于心肺转流系统的血液管路。
注:过滤器适用于进行心肺转流手术时,滤除人体血液中的各种微粒,如血块、碎屑和气栓及其他具有潜在性危险的物质。

Publish Date: 2024-07-08

YY 0117.2-2024 Pending

YY 0117.2-2024 Implants for surgery—Forgings,castings for bone joint prostheses—Part 2:ZTi6Al4V titanium alloy castings

本文件规定了由ZTi6Al4V钛合金材料制造的外科植入物骨关节假体铸件的要求、试验方法、检验规则、质量证明、标记、包装、运输和贮存。
本文件适用于骨关节假体ZTi6Al4V钛合金铸件的生产和验收。

Publish Date: 2024-07-08

YY 0117.3-2024 Pending

YY 0117.3-2024 Implants for surgery—Forgings,castings for bone joint prostheses—Part 3:Cobalt chromium molybdenum alloy castings

本文件规定了外科植入物用钴铬钼合金材料制造外科植入物骨关节假体铸件的要求、试验方法、 检验规则、质量证明、标记、包装、运输和贮存。
本文件适用于骨关节假体钴铬钼金铸件的生产和验收。

Publish Date: 2024-07-08