Current Category: CN-YY - Medicine
This part of YY 0290 specifies the basic requirements for all types of intraocular lenses used in surgical implantation in the human anterior segment, excluding corneal implants and grafts.
Except for the following content, this chapter of the general standard applies.
Addition:
This dedicated standard specifies the requirements for the safety and basic performance of automatic cyclic non-invasive blood pressure monitoring devices defined in 2.102. This dedicated standard will hereinafter refer to automatic cyclic non-invasive blood pressure monitoring devices as "devices". The devices may be either attended devices or unattended devices.
This dedicated standard does not apply to blood pressure measurement devices that use finger sensors or semi-automatic blood pressure measurement devices that require manual activation for each measurement.
This dedicated standard applies to the safety requirements of multi-parameter patient monitoring devices as defined in 2.2.101.
The scope of this standard is limited to devices that have more than one application component or more than one single function, and are connected to a single patient.
This standard does not specify requirements for individual monitoring functions.
This standard specifies the safety and effectiveness requirements for all automatic and electronic arterial blood pressure monitors that use occlusion cuffs to measure indirect arterial blood pressure in humans.
This standard specifies the requirements and test methods for ophthalmometry instruments.
This standard specifies the requirements and test methods for ophthalmological examination heads used to measure the binocular vision function and refractive errors of the human eye.
This standard specifies the general requirements and test methods for silicone rubber tubing (hereinafter referred to as "tubing") and elastic parts used in infusion and blood transfusion.
The present part of YY 0068 specifies the mechanical performance requirements and test methods for rigid endoscopes.
This part is applicable to rigid endoscopes used for medical purposes.
This part of YY 0068 specifies the requirements for the labeling and accompanying documentation of rigid endoscopes.
This standard specifies the requirements, test methods, inspection rules, marking, packaging, transportation, and storage of polyethylene special materials for medical infusion, blood transfusion, and injection equipment. This standard applies to polyethylene special materials for medical infusion, blood transfusion, and injection equipment (hereinafter referred to as "medical polyethylene special materials").
This standard specifies the packaging, marking, and user manuals for surgical instrument products. This standard applies to the general packaging, disinfection packaging, and sterile packaging of surgical instrument products.
This standard specifies the classification and types of nasal endoscopes, their requirements, test methods, inspection rules, marking, user manuals, packaging, transportation, and storage.
This standard applies to nasal endoscopes for examination and surgical use. Examination nasal endoscopes are used for nasal cavity examination, while surgical nasal endoscopes are used for examination and surgery of the nasal cavity and turbinates.