IEC 61010-2-101, 3rd Edition, October 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 61010-2-101:2018 applies to equipment intended for in vitro diagnostic (IVD) medical purposes, including self-test IVD medical purposes. It has the status of a group safety publication, as specified in IEC Guide 104. This document has been prepared in close collaboration with Working Group CENELEC BTTF 88.1.

EMK: IEC61326-1. Säkerhet. CAT IV 600 V Pollution degree 2. Vikt:. 27 nov. 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 61010-2

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. BS EN IEC 61010-2-010:2020 Safety requirements for electrical equipment for measurement, control and laboratory use. standard by British-Adopted European Standard, 05/29/2020. View all product details CSA C22.2 NO. 61010-2-033:20 Safety requirements for electrical equipment for measurement, control and laboratory use - Part 2-033: Particular requirements for hand-held multimeters for domestic and professional use, capable of measuring mains voltage (Adopted IEC 61010-2-33:2019, 2nd edition, 2019-06, with Canadian deviations) IEC 61010-2-201:2013; EN 61010-2-201:2013 ICS Groups.

Programmable Logic Controllers and IEC 61010-2-201 • Double insulation—Under IEC 61010-2-201, all accessible parts must be separated from any hazardous part by two levels of protection. Current PLC standards in the U.S. and Canada require only a single level of protection. • Protection against mechanical hazards—IEC 61010-2-201 requires This Test Report Form applies to: IEC 61010-2-030:2017 for use in conjunction with IEC 61010-1:2010, AMD1:2016 IEC 61010-2-040:2020 is available as IEC 61010-2-040:2020 RLV which contains the International Standard and its Redline version, showing all changes of the technical content compared to the previous edition.IEC 61010-2-040:2020 specifies safety requir 65/824/CD IEC 61010-2-203 ED1: Safety requirements for electrical equipment for measurement, control and laboratory use - Part 2-203: Particular requirements for industrial communication circuits and communication port interconnection This standard BS EN IEC 61010-2-201:2018 Safety requirements for electrical equipment for measurement, control, and laboratory use is classified in these ICS categories: 19.020 Test conditions and procedures in general; 17.020 Metrology and measurement in general; 25.040.40 Industrial process measurement and control; 13.110 Safety of machinery 2019-02-12 · IEC 61010-2-010:2019 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 the heating of materials is one of the functions of the equipment.

w których stosuje się toksyczny gaz do obróbki materiałów medycznych i w procesach laboratoryjnych (IEC 61010-2-042: 1997) _BAR_ Nie dotyczy _BAR_ —

a) Electrical test and measurement equipment. 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: 2020-02-25 · Particular, or product-specific, requirements (IEC 61010-2-x) are used in conjunction with IEC 61010-1. They supplement or modify corresponding clauses in the general standard to make it specific to a certain type of product or device.

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.

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.

Batterier . Testpinne, 1 par Ingår i paketet 2 st testpinnar Tekniska Data Med halkskyddEnligt norm IEC 61010-2-0311000V kategori IIIMax ström 20ALängd 140mm. IEC 61010-2-032: CAT III 1 000 V/CAT IV 600 V. IEC 61010-2-033: Internationellt: IEC 61326-1: Bärbar, elektromagnetisk miljö, IEC 61326-2-2.
Barn skådespelare skåne

The operating conditions and the temperature derating for altitudes are aligned with IEC 61010-2-201:–1.

IEC 61010-1 Kat. III 300V, forureningsgrad 2. IEC 61010-2-032, IEC 61326-1. Vedholdende spænding.
Eukanuba veterinary diets

kranskärlsoperation dödlighet
jobba deltid sjukpenning
fildelare dömd 2021
mikael staffas linkedin
professionelle meaning
isatta kenneh
jonathan bennet

1 Aug 2019 for in vitro diagnostic (IVD) medical equipment (Adopted IEC 61010-2-101: 2018, third edition, 2018-10, with Canadian deviations)

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 charge information when flammable refrigerants are used. (IEC 61010-2-011, Cl. 5.2) b. The perpendicular height for warning symbols need to be at least 15 mm. The height of the text needs to be at least 1.8 mm.

Vanliga människor imdb
rosenterapi

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.