ZH
RU
ES
ivd in vitro
ivd in vitro, Total:47 items.
In the international standard classification, ivd in vitro involves: Electricity. Magnetism. Electrical and magnetic measurements, Medical equipment, Electromagnetic compatibility (EMC), Laboratory medicine, Electrical and electronic testing, Industrial automation systems, Analytical chemistry.
British Standards Institution (BSI), ivd in vitro
- BS EN IEC 61326-2-6:2021 Electrical equipment for measurement, control and laboratory use. EMC requirements. Particular requirements. In vitro diagnostic (IVD) medical equipment
- BS EN IEC 61010-2-101:2022+A11:2022 Safety requirements for electrical equipment for measurement, control, and laboratory use - Safety requirements for in vitro diagnostic (IVD) medical equipment
- BS EN 61326-2-6:2013 Electrical equipment for measurement, control and laboratory use. EMC requirements. Particular requirements. In vitro diagnostic (IVD) medical equipment
- BS EN 61010-2-101:2017 Tracked Changes. Safety requirements for electrical equipment for measurement, control and laboratory use. Particular requirements for in vitro diagnostic (IVD) medical equipment
- 18/30374801 DC BS EN 61326-2-6. Electrical equipment for measurement, control and laboratory use. EMC requirements. Part 2-6. Particular requirements. In vitro diagnostic (IVD) medical equipment
- 21/30438910 DC BS EN 61010-2-101. Safety requirements for electrical equipment for measurement, control, and laboratory use. Part 2-101. Safety requirements for in vitro diagnostic (IVD) medical equipment
Association Francaise de Normalisation, ivd in vitro
- NF EN IEC 61326-2-6:2021 Matériel électrique de mesure, de commande et de laboratoire - Exigences relatives à la CEM - Partie 2-6 : exigences particulières - Matériel médical de diagnostic in vitro (IVD)
- NF C46-050-2-6*NF EN IEC 61326-2-6:2021 Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6 : particular requirements - In vitro diagnostic (IVD) medical equipment
- NF C46-050-2-6*NF EN 61326-2-6:2013 Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6 : particular requirements - In vitro diagnostic (IVD) medical equipment
- NF EN IEC 61010-2-101/A11:2022 Exigences de sécurité pour appareils électriques de mesurage, de régulation et de laboratoire - Partie 2-101 : Exigences particulières pour le matériel médical de diagnostic in vitro (DIV)
- NF EN IEC 61010-2-101:2022 Exigences de sécurité pour appareils électriques de mesurage, de régulation et de laboratoire - Partie 2-101 : exigences particulières pour le matériel médical de diagnostic in vitro (DIV)
- NF C42-020-2-101*NF EN 61010-2-101:2017 Safety requirements for electrical equipment for measurement, control and laboratory use - Part 2-101 : particular requirements for in vitro diagnostic (IVD) medical equipment
International Organization for Standardization (ISO), ivd in vitro
- ISO 20916:2019 In vitro diagnostic medical devices — Clinical performance studies using specimens from human subjects — Good study practice
Danish Standards Foundation, ivd in vitro
- DS/EN IEC 61326-2-6:2021 Electrical equipment for measurement, control and laboratory use – EMC requirements – Part 2-6: Particular requirements – In vitro diagnostic (IVD) medical equipment
European Committee for Electrotechnical Standardization(CENELEC), ivd in vitro
- EN IEC 61326-2-6:2021 Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment
- EN IEC 61010-2-101:2022/prAB Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-101 Particular requirements for in vitro diagnostic (IVD) medical equipment
- EN IEC 61010-2-101:2022/A11:2022 Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-101: Safety requirements for in vitro diagnostic (IVD) medical equipment
- EN IEC 61010-2-101:2022 Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-101: Safety requirements for in vitro diagnostic (IVD) medical equipment
ES-UNE, ivd in vitro
- UNE-EN 61326-2-6:2013 Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment (Endorsed by AENOR in June of 2013.)
- UNE-EN 61010-2-101:2018 Safety requirements for electrical equipment for measurement, control and laboratory use - Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment
- UNE-EN IEC 61010-2-101:2023 Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-101: Safety requirements for in vitro diagnostic (IVD) medical equipment
- UNE-EN IEC 61010-2-101:2023/A11:2023 Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-101: Safety requirements for in vitro diagnostic (IVD) medical equipment
Japanese Industrial Standards Committee (JISC), ivd in vitro
- JIS C 61326-2-6:2023 Electrical equipment for measurement, control and laboratory use -- EMC requirements -- Part 2-6: Particular requirements -- In vitro diagnostic (IVD) medical equipment
- JIS C 1010-2-101:2013 Safety requirements for electrical equipment for measurement, control and laboratory use -- Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment
- JIS C 1010-2-101:2017 Safety requirements for electrical equipment for measurement, control and laboratory use -- Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment
- JIS C 1806-2-6:2012 Electrical equipment for measurement, control and laboratory use -- EMC requirements -- Part 2-6: Particular requirements -- In vitro diagnostic (IVD) medical equipment
- JIS C 61326-2-6:2019 Electrical equipment for measurement, control and laboratory use -- EMC requirements -- Part 2-6: Particular requirements -- In vitro diagnostic (IVD) medical equipment
RU-GOST R, ivd in vitro
- GOST R IEC 61326-2-6-2014 Electrical equipment for measurement, control and laboratory use. EMC requirements. Part 2-6. Particular requirements. In vitro diagnostic (IVD) medical equipment
- GOST IEC 61010-2-101-2013 Safety requirements for electrical equipment for measurement, control and laboratory use. Part 2-101. Particular requirements for in vitro diagnostic (IVD) medical equipment
Professional Standard - Medicine, ivd in vitro
- YY 0648-2008 Safety requirments for electrical equipment for measurement,control and laboratory use.Part 2-101:Particular requirments for in vitro diagnostic(IVD)medical equipment
German Institute for Standardization, ivd in vitro
- DIN EN 61010-2-101:2003 Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment (IEC 61010-2-101:2002, modified); German version EN 61010-2-101:2002
- DIN EN 61326-2-6:2013 Electrical equipment for measurement, control and laboratory use - EMC requirements.Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment (IEC 61326-2-6:2012); German version EN 61326-2-6:2013
- DIN EN 61326-2-6 Berichtigung 1:2008 Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment (IEC 61326-2-6:2005); German version EN 61326-2-6:2006, Corrigendum to DIN EN 61326-2-6 (
International Electrotechnical Commission (IEC), ivd in vitro
- IEC 61326-2-6:2020 Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment
- IEC 61010-2-101:2018 RLV Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment
- IEC 61326-2-6:2020 RLV Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment
- IEC 61326-2-6/COR1:2007 Electrical equipment for measurement, control and laboratory use, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In-vitro diagnostic (IVD) medical equipment; Corrigendum 1
AENOR, ivd in vitro
- UNE-EN 61010-2-101:2004 Safety requirements for electrical equipment for measurement, control and laboratory use -- Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment
General Administration of Quality Supervision, Inspection and Quarantine of the People‘s Republic of China, ivd in vitro
- GB/T 18268.26-2010 Electrical equipment for measurement,control and laboratory use.EMC requirements.Part 26:Particular requirements.In vitro diagnostic(IVD) medical equipment
Lithuanian Standards Office , ivd in vitro
- LST EN 61326-2-6-2006 Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment (IEC 61326-2-6:2005)
- LST EN IEC 61326-2-6:2021 Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment (IEC 61326-2-6:2020)
- LST EN 61010-2-101-2003 Safety requirements for electrical equipment for measurement, control, and laboratory use. Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment (IEC 61010-2-101:2002, modified)
PL-PKN, ivd in vitro
- PN-EN IEC 61326-2-6-2021-11 E Electrical equipment for measurement, control and laboratory use -- EMC requirements -- Part 2-6: Particular requirements -- In vitro diagnostic (IVD) medical equipment (IEC 61326-2-6:2020)
Underwriters Laboratories (UL), ivd in vitro
- UL 61010-2-101-2015 UL Standard for Safety Safety Requirements for Electrical Equipment for Measurement@ Control and Laboratory Use – Part 2-101: Particular Requirements for In Vitro Diagnostic (IVD) Medical Equipment (Second Edition)
- UL 61010-2-101 BULLETIN-2015 UL Standard for Safety Electrical Equipment for Measurement@ Control@ and Laboratory Use – Part 2-101: Particular Requirements for In Vitro Diagnostic (IVD) Medical Equipment (COMMENTS DUE: JULY 27@ 2015)
- UL 61010-2-101 BULLETIN-2019 UL Standard for Safety for Safety Requirements for Electrical Equipment for Measurement@ Control and Laboratory Use - Part 2-101: Particular Requirements for In Vitro Diagnostic (IVD) Medical Equipment (COMMENTS DUE: JUNE 17@ 2019)
IX-EU/EC, ivd in vitro
- MEDDEV 2.14/3-2007 GUIDELINES ON MEDICAL DEVICES IVD GUIDANCES: Supply of Instructions For Use (IFU) and other information for In-vitro Diagnostic (IVD) Medical Devices A GUIDE FOR MANUFACTURERS AND NOTIFIED BODIES