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Homepage>BS Standards>11 HEALTH CARE TECHNOLOGY>11.080 Sterilization and disinfection>BS EN IEC 61010-2-081:2020 Safety requirements for electrical equipment for measurement, control and laboratory use Particular requirements for automatic and semi-automatic laboratory equipment for analysis and other purposes
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immediate downloadReleased: 2024-05-08
BS EN IEC 61010-2-081:2020 Safety requirements for electrical equipment for measurement, control and laboratory use Particular requirements for automatic and semi-automatic laboratory equipment for analysis and other purposes

BS EN IEC 61010-2-081:2020

Safety requirements for electrical equipment for measurement, control and laboratory use Particular requirements for automatic and semi-automatic laboratory equipment for analysis and other purposes

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Standard number:BS EN IEC 61010-2-081:2020
Pages:20
Released:2024-05-08
ISBN:978 0 580 99177 6
Status:Standard
DESCRIPTION

BS EN IEC 61010-2-081:2020


This standard BS EN IEC 61010-2-081:2020 Safety requirements for electrical equipment for measurement, control and laboratory use is classified in these ICS categories:
  • 11.080 Sterilization and disinfection
  • 19.080 Electrical and electronic testing
  • 71.040.10 Chemical laboratories. Laboratory equipment
This clause of Part 1 is applicable except as follows: 1.1.1 Equipment included in scope Replacement: Replace the text, except the first paragraph, by the following new text: This part of IEC 61010 applies to automatic and semi-automatic laboratory equipment for analysis and other purposes. Automatic and semi-automatic laboratory equipment consists of instruments or systems for measuring or modifying one or more characteristics or parameters of samples, performing the complete process or parts of the process without manual intervention. Equipment forming part of such a system is within the scope of this document. Examples of equipment within the scope of this document include: - analytical equipment; - automatic sampler (pipettor, aliquoter); - equipment for sample replication and amplification. NOTE 1 In the case of analytical equipment, the complete process usually includes the following steps: - taking a specific quantity of the sample; - preparing the sample by chemical, thermal, mechanical or other means; - measurement; - display, transmission or printing of the results of measurement. NOTE 2 If all or part of the equipment falls within the scope of one or more other Part 2 documents of IEC 61010 as well as within the scope of this document, consideration is given to those other Part 2 documents. 1.1.2 Equipment excluded from scope Addition: Add the following new item: aa) IEC 61010-2-101 (in vitro diagnostic (IVD) equipment). 1.2 Object 1.2.1 Aspects included in scope Addition: Add the following new items: aa) biohazards; bb) hazardous chemical substances. 1.2.2 Aspects excluded from scope Addition: Add the following new item and note: aa) handling or manipulation of material outside the equipment. NOTE Requirements covering these subjects are the responsibility of committees preparing the relevant standards.