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1 Prezentul standard stabile?te clasificarea ?i terminologia specific? instrumentelor medi-cale de uz uman. 2 Instrumentul medical este o pies
MEDICAL INSTRUMENTS Clasification and terminology
Guidelines for the Classification of Medical Devices Rev 8
本规则适用的心电图机是指提供可取下供诊断用的心电图图谱的心电图机，包括心电向量图机和负荷测试仪
Specifies procedures for the conduct and performance of clinical investigations of medical devices. Not applicable to in vitro diagnostic medical
Clinical investigations of medical devices for human subjects - General requirements
YY/T 0606的本部分规定了组织工程医疗产品分类标准的相关方面，以保证组织工程医疗产品对病人和使用者的安全和有效性。本部分不包括传统意义上的器官和组织移植以及活细胞治疗。 本部分适用于组织工程产品的分类要求，不包括其他标准中包括的特定内容
Tissue engineered medical products.Part 3:General classification
来自第267页
Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devices — Part 1: Critical and semi-critical medical devices
Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 1: Critical and semi-critical medical devices (ISO 17664-1:2021)
Tracked Changes. Processing of health care products. Information to be provided by the medical device manufacturer for the processing of medical devices. Critical and semi-critical medical devices
Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devices — Part 1: Critical and semi-critical medical devices
本规则适用于空心纤维透析器，该产品是配合血液透析装置供急慢性肾功能衰竭等患者进行血液透析用的医疗器械
本规则适用于血液透析装置，是供急慢性肾功能衰竭等患者作血液透析治疗时使用的医疗器械
1 Prezentul standard stabile?te clasificarea ?i terminologia specific? instrumentelor medi-cale de uz uman. 2 Instrumentul medical este o pies
MEDICAL INSTRUMENTS Clasification and terminology
Guidelines for the Classification of Medical Devices Rev 8
本规则适用的心电图机是指提供可取下供诊断用的心电图图谱的心电图机，包括心电向量图机和负荷测试仪
Specifies procedures for the conduct and performance of clinical investigations of medical devices. Not applicable to in vitro diagnostic medical
Clinical investigations of medical devices for human subjects - General requirements
YY/T 0606的本部分规定了组织工程医疗产品分类标准的相关方面，以保证组织工程医疗产品对病人和使用者的安全和有效性。本部分不包括传统意义上的器官和组织移植以及活细胞治疗。 本部分适用于组织工程产品的分类要求，不包括其他标准中包括的特定内容
Tissue engineered medical products.Part 3:General classification
来自第267页
Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devices — Part 1: Critical and semi-critical medical devices
Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 1: Critical and semi-critical medical devices (ISO 17664-1:2021)
Tracked Changes. Processing of health care products. Information to be provided by the medical device manufacturer for the processing of medical devices. Critical and semi-critical medical devices
Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devices — Part 1: Critical and semi-critical medical devices
本规则适用于空心纤维透析器，该产品是配合血液透析装置供急慢性肾功能衰竭等患者进行血液透析用的医疗器械
本规则适用于血液透析装置，是供急慢性肾功能衰竭等患者作血液透析治疗时使用的医疗器械
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