Standards

YY 0697-2008 Replaced

YY 0697-2008 Dynamoelectric traction-table

This standard specifies the requirements, test methods, inspection rules, and marking, packaging, transportation, and storage for electric traction beds (hereinafter referred to as traction beds). This standard applies to equipment used for traction therapy on patients' cervical and lumbar spine regions.

Publish Date: 2008-10-17

YY/T 0010-2008 Replaced

YY/T 0010-2008 Particular specifications for X-ray unit for oral cavity

This standard specifies the terminology, classification, requirements, and test methods for oral X-ray machines (hereinafter referred to as oral machines).
This standard applies to oral machines, which are used by medical units for dental X-ray photography.
This standard does not apply to dental cranial X-ray equipment.

Publish Date: 2008-10-17

YY/T 0106-2008 Replaced

YY/T 0106-2008 General specifications for medical diagnostic X-ray equipment

This standard specifies the classification, requirements, and test methods for medical diagnostic X-ray machines (hereinafter referred to as X-ray machines).
This standard applies to medical diagnostic X-ray machines. For medical diagnostic X-ray machines subject to national or industry-specific standard requirements, it is recommended to comply with the corresponding national or industry-specific standards.
This standard does not apply to X-ray computed tomography equipment.

Publish Date: 2008-10-17

YY/T 0290.1-2008 Replaced

YY/T 0290.1-2008 Ophthalmic implants—Intraocular lenses—Part 1:Terminology

This part of YY 0290 specifies the terminology used for intraocular lenses and their testing.

Publish Date: 2008-10-17

YY/T 0290.4-2008 Replaced

YY/T 0290.4-2008 Ophthalmic implants—Intraocular lenses—Part 4:Labeling and information

This part of YY 0290 specifies the requirements for the information provided on or within the label and packaging of intraocular lenses (IOLs).

Publish Date: 2008-10-17

YY/T 0686-2008 Replaced

YY/T 0686-2008 Medical forceps

This standard specifies the types and nomenclature of medical forceps, as well as their requirements, test methods, inspection rules, marking, packaging, transportation, and storage.
This standard applies to medical forceps used for grasping tissues and dressings.

Publish Date: 2008-10-17

YY/T 0688.1-2008 Replaced

YY/T 0688.1-2008 Clinical laboratory testing and in vitro diagnostic test systems—Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility devices—Part 1:Reference method for testing the in vitro activity of antimicrobial agents against rapidly growing aerobic bacteria involved in infectious diseases

This part of YY/T 0688 introduces a reference method for determining the MIC value of antimicrobial agents—the broth microdilution method. The MIC value only reflects the antibacterial activity of the antimicrobial agent under the specified in vitro test conditions. When formulating a medication regimen, doctors should not only refer to the MIC results, but also consider other factors such as the pharmacokinetic/pharmacodynamic parameters of the drug in the human body and the bacterial resistance mechanisms to the antimicrobial agent. For a certain antimicrobial agent, the corresponding test bacteria can be divided into "sensitive (S)", "intermediate (I)" and "resistant (R)" according to the results of the in vitro sensitivity test (MIC value). In addition, the MIC value can be used to determine whether the test strain is a wild-type or non-wild-type. Although interpreting the clinical significance of the MIC value is beyond the scope of this part, it is necessary to adjust the basic content of the method according to different combinations of antimicrobial agents and bacteria to meet clinical needs. These adjustments are reflected in the following tables. To ensure the comparability and reliability of the test results, other antimicrobial susceptibility testing methods (such as conventional methods or antimicrobial susceptibility testing equipment) should be compared with this reference method to determine their accuracy.

Publish Date: 2008-10-17

YY/T 0694-2008 Replaced

YY/T 0694-2008 Standard test method for measuring intrinsic elastic recoil of balloon-expandable stents

1.1 The purpose of this test method is to quantify the expansion diameter of the stent on the balloon and the post-decompression diameter of the stent after the balloon is removed, as well as the stent diameter retraction rate. This test method is suitable for stents made of materials that can undergo plastic deformation under mechanical action before and after expansion. This test method can be carried out at room temperature, unless certain materials have special temperature requirements. The test temperature should be specified in the report (if applicable). 1.2 This standard does not cover all safety issues related to use. It is the responsibility of the users of this standard to determine its applicability by establishing appropriate safety and health evaluation mechanisms before use.

Publish Date: 2008-10-17

YY/T 0696-2008 Replaced

YY/T 0696-2008 Test method for measuring output characteristics of the nerve and muscle stimulators

This standard specifies the measurement methods for the output characteristics of equipment within the scope of application of YY 0607—2007, and at the same time, unifies the understanding of the relevant provisions of YY 0607—2007.

Publish Date: 2008-10-17

YY/T 0701-2008 Replaced

YY/T 0701-2008 Calibrator for hematology analyzer

This standard specifies the terms and definitions, naming and classification, technical requirements, test methods, inspection rules, marking, labels and instructions, packaging, transportation, and storage of calibrators used in blood cell analyzers (hereinafter referred to as calibrators).
This standard applies to calibrators used in blood cell analyzers. These calibrators are used to calibrate the five parameters of WBC, RBC, HGB, MCV/HCT, and PLT in blood cell analyzers (also known as hematology analyzers), thereby establishing the metrological traceability of the measurement results of blood cell analyzers.

Publish Date: 2008-10-17

YY/T 0706-2008 Replaced

YY/T 0706-2008 Particular specifications for mammographic X-ray equipment

This standard specifies the terminology, classification, requirements, and test methods for breast X-ray machines (hereinafter referred to as breast X-ray machines).
This standard applies to breast X-ray machines that use X-ray film intensifying screens and operate in either contact or magnified modes, and are specifically designed for use in medical units for breast X-ray photography.
This standard does not apply to specialized accessories such as digital imaging devices, biopsy plates, and stereotactic positioning devices.

Publish Date: 2008-10-17

YY/T 0707-2008 Replaced

YY/T 0707-2008 Particular specifications for mobile radiography X-ray equipment

This standard specifies the terminology, classification, and composition, requirements, and test methods for portable photographic X-ray machines (hereinafter referred to as X-ray machines).
This standard is only applicable to X-ray machines dedicated for photographic purposes, powered by single-phase AC power and/or internal power sources.

Publish Date: 2008-10-17