Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-0...
IEC 61010-2-012:2016 specifies safety requirements for electrical equipment and their accessories within the categories a) through c), wherever they are intended to be used, whenever that equipment incorporates one or more of the following characteristics:
- A REFRIGERATING SYSTEM that is acted on or impacted by an integral heating function such that the combined heating and cooling system…
Clinical laboratory testing and in vitro diagnostic test systems — Reference method for testing the ...
ISO 16256:2012 describes a method for testing the susceptibility to antifungal agents of yeasts, including Candida spp. and Cryptococcus neoformans, that cause infections. The reference method described here has not been used in studies of the yeast forms of dimorphic fungi, such as B. dermatitidis and/or H. capsulatum variety capsulatum.
ISO 16256:2012 describes the broth microdilution…
Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6: Part...
IEC 61326-2-6:2012 specifies minimum requirements for immunity and emissions regarding electromagnetic compatibility for in vitro diagnostic medical equipment, taking into account the particularities and specific aspects of this electrical equipment and their electromagnetic environment. This second edition cancels and replaces the first edition published in 2005 and constitutes a technical…
Clinical laboratory testing and in vitro diagnostic test systems — In vitro diagnostic medical devic...
ISO/TR 18112:2006 summarizes regulatory requirements and associated guidance for information supplied by the manufacturer with IVD medical devices intended for professional use.
Information supplied by the manufacturer includes labels on the outer and immediate container as well as instructions for use.
Current labelling regulations and regulatory guidance from Canada, the European Union, Japan…
Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6: Part...
specifies minimum requirements for immunity and emissions regarding electromagnetic compatibility for in vitro diagnostic medical equipment, taking into account the particularities and specific aspects of this electrical equipment and their electromagnetic environment.
The contents of the corrigendum of September 2007 have been included
in this copy.
Acoustics — Laboratory tests on noise emission from appliances and equipment used in water supply in...
Gives the mounting and operating conditions to be used for a number of in-line valves and appliances, when measuring the noise emission resulting from water flow. Replaces the first edition.
Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-0...
Applies to hand-held and hand-manipulated CURRENT CLAMPS. These CURRENT CLAMPS are for use in the measurement of current without interruption of the current path of the circuit in which it is measured. They may be stand-alone CURRENT CLAMPS which are themselves within the scope of part 1, or accessories to other equipment within the scope of part 1. This standard does not apply to current…
Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-0...
Applies to the following hand-held and hand-manipulated probe assemblies: -low-voltage and high-voltage, non-attenuating probe assemblies (type A) -high-voltage attenuating or divider probe assemblies (type B) -low-voltage attenuating or divider probe assemblies (type C). Has the status of a group safety publication in accordance with IEC Guide 104.