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ivd device

ivd device, Total:60 items.

In the international standard classification, ivd device involves: Laboratory medicine, Electricity. Magnetism. Electrical and magnetic measurements, Medical equipment, Electromagnetic compatibility (EMC), Electrical and electronic testing, Industrial automation systems, Analytical chemistry.

British Standards Institution (BSI), ivd device

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 61010-2-101:2002 Safety requirements for electrical equipment for measurement, control and laboratory use - Particular 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 61326-2-6:2006 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 device

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
NF C42-739:2003 Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-101 : particular requirements for in vitro diagnostic (IVD) medical equipment.
NF C46-050-2-6:2006 Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6 : particular requirements - In-vitro diagnostic (IVD) medical equipment.

Danish Standards Foundation, ivd device

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 device

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
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
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
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 (Remains Current)
EN 61010-2-101:2002 Safety requirements for electrical equipment for measurement, control, and laboratory use Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment

ES-UNE, ivd device

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 device

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

Professional Standard - Medicine, ivd device

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 device

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 device

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 61010-2-101:2015 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 Safety requirements for electrical equipment for measurement, control and laboratory use - Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment
IEC 61010-2-101:2018 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 61326-2-6:2005 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
IEC 61326-2-6:2012 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 device

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

RU-GOST R, ivd device

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

General Administration of Quality Supervision, Inspection and Quarantine of the People‘s Republic of China, ivd device

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

ZA-SANS, ivd device

SANS 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

Lithuanian Standards Office , ivd device

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 device

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)

International Organization for Standardization (ISO), ivd device

ISO 20916:2019 In vitro diagnostic medical devices — Clinical performance studies using specimens from human subjects — Good study practice

Underwriters Laboratories (UL), ivd device

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 device

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