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nostic (IVD) medical equipment[24] IEC/TR3 610103, Safety requirements for electrical equipment for measurement, control, and laboratory use — Part 3: Protocol for the preparation of conformity verification reports for the IEC 61010 series[25] IEC/TR3 6101031, Safety requirements for electrical equipment for measurement, control, and laboratory use — Part 31: Conformity verification report for IEC 610101[26] IEC/TR 610103010, Safety requirements for electrical equipment for measurement, control, and laboratory use — Part 3010: Conformity verification report for IEC 610102010, Particular requirements for laboratory equipment for the heating of materials[27] IEC/TR 610103020, Safety requirements for electrical equipment for measurement, control, and laboratory use — Part 3020: Conformity verification report for IEC 610102020, Particular requirements for laboratory centrifuges[28] IEC/TR 610103051, Safety requirements for electrical equipment for measurement, control, and laboratory use — Part 3051: Conformity verification report for IEC 610102051, Particular requirements for laboratory equipment for mixing and stirring[29] IEC/TR 610103061, Safety requirements for electrical equipment for measurement, control, and laboratory use — Part 3061: Conformity verification report for IEC 610102061, Particular requirements for laboratory atomic spectrometers with thermal atomization and ionization[30] IUPACIPCS Chemical Safety Matters, International Union of Pure and Applied Chemistry,1992[31] ISO/IEC Guide 63, Guide to the development and inclusion of safety aspects in International Standards for medical devices[32] ISO/IEC Guide 51, Safety aspects — Guidelines for their inclusion in standards[33] NCCLS GP5A, Clinical laboratory waste management。 Approved guideline. 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