Utfärdat okt 2015. IEC/EN 60335-1-bild. IEC/EN 60335-1. Intertek Semko AB. Utfärdat sep 2015. IEC 61010-2-XX-bild Utfärdat sep 2014. IEC 61010-1-bild
IEC. 61010-2-081. 2001. AMENDMENT 1. 2003-06. Amendment 1. Safety requirements for electrical equipment for measurement, control, and laboratory use –.
は、2020年4月30日に廃止された。本規格がリリ－スされてから廃止になるまで 約3年半の短い期間であった。 IEC 61010-2-201:2017 specifies safety requirements and related verification tests for any product performing the function of control equipment and/or their associated peripherals. In addition, these products have as their intended use the command and control of machines, automated manufacturing and industrial processes, e.g. discrete and continuous control. IEC 61010-2-040:2020 specifies safety requirements for electrical equipment intended for sterilization, washing, and disinfection of medical materials in the medical, veterinary, pharmaceutical and laboratory fields, when used under the environmental conditions of 1.4. Examples of such equipment include the following: IEC 61010-2-101:2015 is available as. IEC 61010-2-101:2015 RLV. which contains the International Standard and its Redline version, showing all changes of the technical content compared to the previous edition.
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discrete and The IEC 61010 2 Standard For Refrigerated Systems In Laboratory Equipment This white paper is about the IEC 61010 family of standards focusing on laboratory equipment. The 2-011:2016 and 2-012:2016 distinctions of the IEC 61010 go in-depth to specifically address refrigerated systems in laboratory equipment. IEC 61010-2-101:2015 is available as IEC 61010-2-101:2015 RLV which contains the International Standard and its Redline version, showing all changes of the technical content compared to the previous edition. IEC 61010-2-101:2015 applies to equipment intended for in vitro diagnostic (IVD) medical purposes, including self-test IVD medical purposes.
This separates IEC 61010-2-081 and IEC 61010-2-101 equipment;
- updated Biohazard and Lot symbols in Table 1 in Clause 5;
- added requirement for within expiration consumables and authorized representative details in Instructions for Use to Clause 5;
- added requirement for gas or liquid markings and ratings to Clause 5;
- added requirement to include OPERATOR
Stöt enligt IEC 60068-2-27. w których stosuje się toksyczny gaz do obróbki materiałów medycznych i w procesach laboratoryjnych (IEC 61010-2-042: 1997) _BAR_ Nie dotyczy _BAR_ — IEC/EN 61010-2-032 utgåva.
IEC-mätkategori III. CAT III-utrustning har skydd mot IEC/EN 61010-1:2001, 600V CAT III, 300V CAT IV. Föroreningsgrad 2. EN/IEC 61010-2-32:2002. EN/IEC
2019 — IEC 61010-2-201:2018 för utrustning för mätning, styrning och laboratorieändamål; EN IEC 61058-1:2018 för strömställare för bruksföremål; Højde 2000m eller lavere, indendørs brug. Standarder. IEC 61010-1 Kat. III 300V, forureningsgrad 2. IEC 61010-2-032, IEC 61326-1.
IEC 61010-2-101:2015 is available as IEC 61010-2-101:2015 RLV which contains the International Standard and its Redline version, showing all changes of the technical content compared to the previous edition. IEC 61010-2-101:2015 applies to equipment intended for in vitro diagnostic (IVD) medical purposes, including self-test IVD medical purposes. iec 61010-2-201 March 1, 2017 Safety requirements for electrical equipment for measurement, control, and laboratory use – Part 2-201: Particular requirements for control equipment
IEC 61010-2-101:2018 applies to equipment intended for in vitro diagnostic (IVD) medical purposes, including self-test IVD medical purposes.
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IEC 61010-2-011:2016 specifies particular safety requirements for the following types a) to c) of electrical equipment and their accessories, wherever they are intended to be used, whenever that equipment incorporates REFRIGERATING SYSTEMS whether an integral part of, or remote to the equipment and the equipment is in direct control of the REFRIGERATING SYSTEM. Abstract IEC 61010-2-091:2012 specifies particular safety requirements for CABINET X-RAY SYSTEMS. IEC 61010-2-040:2020 specifies safety requirements for electrical equipment intended for sterilization, washing, and disinfection of medical materials in the medical, veterinary, pharmaceutical and laboratory fields, when used under the environmental conditions of 1.4. Examples of such equipment include the following: IEC 61010 is the electrical requirements for laboratory test and measurement equipment… The equipment and machines used to measure, control and for use in labs within your facility or in your client’s facility, control of process output variables, temperature controllers, pH controllers…things of that nature. IEC 61010-2-201:2017 specifies safety requirements and related verification tests for any product performing the function of control equipment and/or their associated peripherals.
IEC 61010-2-010:2019 is available as IEC 61010-2-010:2019 RLV which contains the International Standard and its Redline version, showing all changes of the technical content compared to the previous edition..
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buy en iec 61010-2-120 : 2018 safety requirements for electrical equipment for measurement, control, and laboratory use - part 2-120: particular safety requirements for machinery aspects of equipment (iec 61010-2-120:2016) from sai global
This separates IEC 61010-2-081 and IEC 61010-2-101 equipment;
- updated Biohazard and Lot symbols in Table 1 in Clause 5;
- added requirement for within expiration consumables and authorized representative details in Instructions for Use to Clause 5;
- added requirement for gas or liquid markings and ratings to Clause 5;
- added requirement to include OPERATOR
IEC 61010-2-201 and include no national deviations.