loading
ASTM G175-13(2021) - Standard Test Method for Evaluating the Ignition Sensitivity and Fault Tolerance of Oxygen Pressure Regulators Used for Medical and Emergency Applications
December 1, 2021 - ASTM International

1.1 For the purpose of this standard, a pressure regulator, also called a pressure-reducing valve, is a device intended for medical or emergency purposes that is used to convert a medical or emergency gas pressure from a high, variable pressure to a lower, more constant working...

ASTM D8320-21 - Standard Practice for Implementing an Information Security Program in a Cannabis Operation
July 1, 2021 - ASTM International

1.1 This practice covers recommendations for implementing an information security program to protect businesses operating in the regulated cannabis industry. An information security program is part of an overall security program that each business should implement. 1.2 This practice applies to any...

CEI EN IEC 60601-2-66 - Medical electrical equipment Part 2-66: Particular requirements for the basic safety and essential performance of hearing aids and hearing aid systems
July 1, 2020 - CEI

This part of IEC 60601 applies to the BASIC SAFETY of HEARING AIDS and HEARING AID SYSTEMS, hereafter also referred to as ME EQUIPMENT or ME SYSTEM. If a clause or subclause is specifically intended to be applicable to HEARING AIDS only, or to HEARING AID SYSTEMS only, the title and content of that...

IEC 60601-2-66 REDLINE - Medical electrical equipment – Part 2-66: Particular requirements for the basic safety and essential performance of hearing aids and hearing aid systems
October 1, 2019 - IEC

This part of IEC 60601 applies to the BASIC SAFETY of HEARING AIDS and HEARING AID SYSTEMS, hereafter also referred to as ME EQUIPMENT or ME SYSTEM. If a clause or subclause is specifically intended to be applicable to HEARING AIDS only, or to HEARING AID SYSTEMS only, the title and content of that...

IEC 60601-2-66 - Medical electrical equipment – Part 2-66: Particular requirements for the basic safety and essential performance of hearing aids and hearing aid systems
October 1, 2019 - IEC

This part of IEC 60601 applies to the BASIC SAFETY of HEARING AIDS and HEARING AID SYSTEMS, hereafter also referred to as ME EQUIPMENT or ME SYSTEM. If a clause or subclause is specifically intended to be applicable to HEARING AIDS only, or to HEARING AID SYSTEMS only, the title and content of that...

IEC 61010-2-101 REDLINE - Safety requirements for electrical equipment for measurement, control and laboratory use – Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment
October 1, 2018 - IEC

Equipment included in scope This part of IEC 61010 applies to equipment intended for in vitro diagnostic (IVD) medical purposes, including self-test IVD medical purposes. IVD medical equipment, whether used alone or in combination, is intended by the manufacturer to be used in...

IEC 61010-2-101 - Safety requirements for electrical equipment for measurement, control and laboratory use – Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment
October 1, 2018 - IEC

Equipment included in scope This part of IEC 61010 applies to equipment intended for in vitro diagnostic (IVD) medical purposes, including self-test IVD medical purposes. IVD medical equipment, whether used alone or in combination, is intended by the manufacturer to be used in...

IEC 61010-2-010 - Safety requirements for electrical equipment for measurement, control and laboratory use – Part 2-010: Particular requirements for laboratory equipment for the heating of materials
February 1, 2019 - IEC

Equipment included in scope This group safety publication is primarily intended to be used as a product safety standard for the products mentioned in the scope, but shall also be used by technical committees in the preparation of their publications for products similar to those mentioned in the...

CEI EN 61010-2-101 - Safety requirements for electrical equipment for measurement, control and laboratory use Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment
August 1, 2017 - CEI

This part of IEC 61010 applies to equipment intended for in vitro diagnostic (IVD) medical purposes, including self-test IVD medical purposes. IVD medical equipment, whether used alone or in combination, is intended by the manufacturer to be used in vitro for the examination of...

CSA C22.2 NO 61010-2-034 - Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-034: Particular requirements for measurement equipment for insulation resistance and test equipment for electric strength
January 1, 2018 - CSA

Equipment included in scope This group safety publication is primarily intended to be used as a product safety standard for the products mentioned in the scope, but shall also be used by technical committees in the preparation of their publications for products similar to those mentioned in the...

CSA C22.2 NO 61010-2-201 - Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-201: Particular requirements for control equipment
January 1, 2018 - CSA

Equipment included in scope This group safety publication is primarily intended to be used as a product safety standard for the products mentioned in the scope, but shall also be used by technical committees in the preparation of their publications for products similar to those mentioned in the...

CEI EN 61010-2-011 - Safety requirements for electrical equipment for measurement, control, and laboratory use Part 2-011: Particular requirements for refrigerating equipment
October 1, 2017 - CEI

Equipment included in scope This part of IEC 61010 specifies general safety requirements for the following types of electrical equipment and their accessories, wherever they are intended to be used. a) Electrical test and measurement equipment This is equipment which by electromagnetic means tests,...

CSA C22.2 NO 61010-2-020 - Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-020: Particular requirements for laboratory centrifuges
January 1, 2017 - CSA

Equipment included in scope This Part 1 applies to test equipment integrated into manufacturing facilities intended for testing electronic devices, including silicon wafers and other semiconductor devices. NOTE This equipment is likely to be installed adjacent to and interconnected with industrial...

CEI EN 50332-1 - Sound system equipment: Headphones and earphones associated with portable audio equipment - Maximum sound pressure level measurement methodology and limit considerations Part 1: General method for "one package equipment"
July 1, 2016 - CEI

The scope of this European Standard is to set up a suitable measuring methodology allowing accurate measurement of the maximum sound pressure level produced by consumer's headphones and earphones when associated with personal music players. NOTE This standard does not apply to acoustically open or...

CEI EN 61010-2-051 - Safety requirements for electrical equipment for measurement, control and laboratory use Part 2-051: Particular requirements for laboratory equipment for mixing and stirring
October 1, 2016 - CEI

This part of IEC 61010 is applicable to electrically operated laboratory equipment and its accessories for mechanical mixing and stirring, where mechanical energy influences the shape or size or homogeneity of materials and their accessories. Such devices may contain heating elements. NOTE If all...

CEI EN 60601-2-66 - Medical electrical equipment Part 2: Particular requirements for the basic safety and essential performance of hearing instruments and hearing instrument systems
July 1, 2016 - CEI

This International Standard applies to the BASIC SAFETY of HEARING INSTRUMENTS and HEARING INSTRUMENT SYSTEMS, hereafter also referred to as ME EQUIPMENT or ME SYSTEM. If a clause or subclause is specifically intended to be applicable to HEARING INSTRUMENTS only, or to HEARING INSTRUMENT SYSTEMS...

IEC 61010-2-020 - Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-020: Particular requirements for laboratory centrifuges
May 1, 2016 - IEC

Equipment included in scope This part of IEC 61010 specifies general safety requirements for the following types of electrical equipment and their accessories, wherever they are intended to be used. a) Electrical test and measurement equipment This is equipment which by electromagnetic means tests,...

IEC 61010-2-020 REDLINE - Safety requirements for electrical equipment for measurement, control, and laboratory use – Part 2-020: Particular requirements for laboratory centrifuges
May 1, 2016 - IEC

Equipment included in scope This part of IEC 61010 specifies general safety requirements for the following types of electrical equipment and their accessories, wherever they are intended to be used. a) Electrical test and measurement equipment This is equipment which by electromagnetic means tests,...

ASTM G175-13 - Standard Test Method for Evaluating the Ignition Sensitivity and Fault Tolerance of Oxygen Pressure Regulators Used for Medical and Emergency Applications
October 1, 2013 - ASTM International

1.1 For the purpose of this standard, a pressure regulator, also called a pressure-reducing valve, is a device intended for medical or emergency purposes that is used to convert a medical or emergency gas pressure from a high, variable pressure to a lower, more constant working...

DS/EN ISO 10651-6 - Lung ventilators for medical use - Particular requirements for basic safety and essential performance - Part 6: Home-care ventilatory support devices
May 11, 2009 - DS

IEC 60601-1:1988, Clause 1 applies, except as follows. Amendment: This part of ISO 10651 specifies the basic safety and essential performance requirements for home-care ventilatory support devices, intended mainly for use in home care but which could be used elsewhere (e.g. in...

Advertisement