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The Government of Canada’s terminology and linguistic data bank.
CAN/CSA-C22.2 NO 61010-2-101:15 [1 record]
Record 1 - internal organization data 2016-05-25
Record 1, English
Record 1, Subject field(s)
- Canadian Standards Association (CSA) Standards
- Security
- Electrical Appliances and Equipment
- Medical Instruments and Devices
Universal entry(ies) Record 1
Record 1, Main entry term, English
- Safety requirements for electrical equipment for measurement, control and laboratory use – Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment
1, record 1, English, Safety%20requirements%20for%20electrical%20equipment%20for%20measurement%2C%20control%20and%20laboratory%20use%20%26ndash%3B%20Part%202%2D101%3A%20Particular%20requirements%20for%20in%20vitro%20diagnostic%20%28IVD%29%20medical%20equipment
correct
Record 1, Abbreviations, English
Record 1, Synonyms, English
Record 1, Textual support, English
Record number: 1, Textual support number: 1 OBS
Canadian version of the standard IEC 61010-2-101:2015. 2, record 1, English, - Safety%20requirements%20for%20electrical%20equipment%20for%20measurement%2C%20control%20and%20laboratory%20use%20%26ndash%3B%20Part%202%2D101%3A%20Particular%20requirements%20for%20in%20vitro%20diagnostic%20%28IVD%29%20medical%20equipment
Record number: 1, Textual support number: 2 OBS
CAN/CSA-C22.2 NO. 61010-2-101:15: standard code used by CSA. 2, record 1, English, - Safety%20requirements%20for%20electrical%20equipment%20for%20measurement%2C%20control%20and%20laboratory%20use%20%26ndash%3B%20Part%202%2D101%3A%20Particular%20requirements%20for%20in%20vitro%20diagnostic%20%28IVD%29%20medical%20equipment
Record 1, Key term(s)
- Particular requirements for in vitro diagnostic (IVD) medical equipment
- Safety requirements for electrical equipment for measurement, control and laboratory use – Part 2-101: Particular requirements for in vitro diagnostic medical equipment
- Safety requirements for electrical equipment for measurement, control and laboratory use – Part 2-101: Particular requirements for IVD medical equipment
- Particular requirements for in vitro diagnostic medical equipment
- Particular requirements for IVD medical equipment
Record 1, French
Record 1, Domaine(s)
- Normes de l'Association canadienne de normalisation (CSA)
- Sécurité
- Appareillage électrique
- Instruments et appareillages médicaux
Entrée(s) universelle(s) Record 1
Record 1, Main entry term, French
- Règles de sécurité pour appareils électriques de mesurage, de régulation et de laboratoire – Partie 2-101 : Exigences particulières pour les appareils médicaux de diagnostic in vitro (DIV)
1, record 1, French, R%C3%A8gles%20de%20s%C3%A9curit%C3%A9%20pour%20appareils%20%C3%A9lectriques%20de%20mesurage%2C%20de%20r%C3%A9gulation%20et%20de%20laboratoire%20%26ndash%3B%20Partie%202%2D101%20%3A%20Exigences%20particuli%C3%A8res%20pour%20les%20appareils%20m%C3%A9dicaux%20de%20diagnostic%20in%20vitro%20%28DIV%29
correct, feminine noun
Record 1, Abbreviations, French
Record 1, Synonyms, French
Record 1, Textual support, French
Record number: 1, Textual support number: 1 OBS
Version canadienne de la norme IEC 61010-2-101:2015. 2, record 1, French, - R%C3%A8gles%20de%20s%C3%A9curit%C3%A9%20pour%20appareils%20%C3%A9lectriques%20de%20mesurage%2C%20de%20r%C3%A9gulation%20et%20de%20laboratoire%20%26ndash%3B%20Partie%202%2D101%20%3A%20Exigences%20particuli%C3%A8res%20pour%20les%20appareils%20m%C3%A9dicaux%20de%20diagnostic%20in%20vitro%20%28DIV%29
Record number: 1, Textual support number: 2 OBS
CAN/CSA-C22.2 NO. 61010-2-101:15 : code de norme utilisé par la CSA. 2, record 1, French, - R%C3%A8gles%20de%20s%C3%A9curit%C3%A9%20pour%20appareils%20%C3%A9lectriques%20de%20mesurage%2C%20de%20r%C3%A9gulation%20et%20de%20laboratoire%20%26ndash%3B%20Partie%202%2D101%20%3A%20Exigences%20particuli%C3%A8res%20pour%20les%20appareils%20m%C3%A9dicaux%20de%20diagnostic%20in%20vitro%20%28DIV%29
Record 1, Key term(s)
- Exigences particulières pour les appareils médicaux de diagnostic in vitro (DIV)
- Règles de sécurité pour appareils électriques de mesurage, de régulation et de laboratoire – Partie 2-101 : Exigences particulières pour les appareils médicaux de diagnostic in vitro
- Règles de sécurité pour appareils électriques de mesurage, de régulation et de laboratoire – Partie 2-101 : Exigences particulières pour les appareils médicaux de DIV
- Exigences particulières pour les appareils médicaux de diagnostic in vitro
- Exigences particulières pour les appareils médicaux de DIV
Record 1, Spanish
Record 1, Textual support, Spanish
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