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CSA CAN/CSA-C22.2 NO. 61010-2-101:04
English -- Safety requirements for electrical equipment for measurement, control and laboratory use – Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment - First Edition;
French -- Règles de sécurité pour appareils électriques de mesurage, de régulation et de laboratoire – Partie 2-101: Prescriptions particulières pour les appareils médicaux de diagnostic in vitro (DIV) - First Edition
Organization:
CSA - CSA Group
Year: 2009
Abstract: Replacement:
This part 2 applies to equipment intended for in vitro diagnostic (IVD) medical purposes, including self-test IVD medical purposes.
IVD medical equipment, whether used alone or in combination, is intended by the manufacturer to be used in vitro for the examination of specimens, including blood and tissue samples, derived from the human body, solely or principally for the purpose of providing information concerning one or more of the following:
• a physiological or pathological state; or
• a congenital abnormality;
• the determination of safety and compatibility with potential recipients; the monitoring of therapeutic measures.
Self-test IVD medical equipment is intended by the manufacturer for use by lay persons in a home environment.
NOTE If all or part of the equipment falls within the scope of one or more other part 2 standards of IEC 61010 as well as within the scope of this standard, it will also need to meet the requirements of those other part 2 standards.
Equipment excluded from scope
Addition:
Add the following second paragraph:
Products for general laboratory use are not IVD medical devices unless such products, in view of their characteristics, are specifically intended by their manufacturer to be used for in vitro diagnostic examination.
This part 2 applies to equipment intended for in vitro diagnostic (IVD) medical purposes, including self-test IVD medical purposes.
IVD medical equipment, whether used alone or in combination, is intended by the manufacturer to be used in vitro for the examination of specimens, including blood and tissue samples, derived from the human body, solely or principally for the purpose of providing information concerning one or more of the following:
• a physiological or pathological state; or
• a congenital abnormality;
• the determination of safety and compatibility with potential recipients; the monitoring of therapeutic measures.
Self-test IVD medical equipment is intended by the manufacturer for use by lay persons in a home environment.
NOTE If all or part of the equipment falls within the scope of one or more other part 2 standards of IEC 61010 as well as within the scope of this standard, it will also need to meet the requirements of those other part 2 standards.
Equipment excluded from scope
Addition:
Add the following second paragraph:
Products for general laboratory use are not IVD medical devices unless such products, in view of their characteristics, are specifically intended by their manufacturer to be used for in vitro diagnostic examination.
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CSA CAN/CSA-C22.2 NO. 61010-2-101:04
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| contributor author | CSA - CSA Group | |
| date accessioned | 2017-09-04T18:24:10Z | |
| date available | 2017-09-04T18:24:10Z | |
| date copyright | 2004.07.01 (R 2009) | |
| date issued | 2009 | |
| identifier other | IFXCDFAAAAAAAAAA.pdf | |
| identifier uri | http://mapnamagz.yabesh.ir/std/handle/yse/206538 | |
| description abstract | Replacement: This part 2 applies to equipment intended for in vitro diagnostic (IVD) medical purposes, including self-test IVD medical purposes. IVD medical equipment, whether used alone or in combination, is intended by the manufacturer to be used in vitro for the examination of specimens, including blood and tissue samples, derived from the human body, solely or principally for the purpose of providing information concerning one or more of the following: • a physiological or pathological state; or • a congenital abnormality; • the determination of safety and compatibility with potential recipients; the monitoring of therapeutic measures. Self-test IVD medical equipment is intended by the manufacturer for use by lay persons in a home environment. NOTE If all or part of the equipment falls within the scope of one or more other part 2 standards of IEC 61010 as well as within the scope of this standard, it will also need to meet the requirements of those other part 2 standards. Equipment excluded from scope Addition: Add the following second paragraph: Products for general laboratory use are not IVD medical devices unless such products, in view of their characteristics, are specifically intended by their manufacturer to be used for in vitro diagnostic examination. | |
| language | English, French | |
| title | CSA CAN/CSA-C22.2 NO. 61010-2-101:04 | num |
| title | English -- Safety requirements for electrical equipment for measurement, control and laboratory use – Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment - First Edition | en |
| title | French -- Règles de sécurité pour appareils électriques de mesurage, de régulation et de laboratoire – Partie 2-101: Prescriptions particulières pour les appareils médicaux de diagnostic in vitro (DIV) - First Edition | other |
| type | standard | |
| page | 58 | |
| status | Active | |
| tree | CSA - CSA Group:;2009 | |
| contenttype | fulltext |