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CEI EN 62353 - Medical electrical equipment - Recurrent test and test after repair of medical electrical equipment
November 1, 2015 - CEI

This International Standard applies to testing of MEDICAL ELECTRICAL EQUIPMENT and MEDICAL ELECTRICAL SYSTEMS, hereafter referred to as ME EQUIPMENT and ME SYSTEMS, or parts of such equipment or systems, which comply with IEC 60601-1:1988 (second edition)...

DS/EN 14683 - Medical face masks – Requirements and test methods
April 1, 2019 - DS

This document specifies construction, design, performance requirements and test methods for medical face masks intended to limit the transmission of infective agents from staff to patients during surgical procedures and other medical settings with similar requirements. A...

DS/EN IEC 62464-1 - Magnetic resonance equipment for medical imaging – Part 1: Determination of essential image quality parameters
March 5, 2019 - DS

This part of IEC 62464 specifies measurement procedures for the determination of many essential image quality parameters for MR EQUIPMENT. Measurement procedures as addressed in this document are suitable for - quality assessment in the ACCEPTANCE TEST, and - quality assurance in the...

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...

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...

DS/ISO 10524-1 - Pressure regulators for use with medical gases – Part 1: Pressure regulators and pressure regulators with flow-metering devices
February 4, 2019 - DS

ISO 10524-1:2018 specifies the design, construction, type testing, and marking requirements for pressure regulators (as defined in 3.18) intended for the administration of medical gases and their mixtures in the treatment, management, diagnostic evaluation and care of patients or for...

DS/EN 62353 - Medical electrical equipment - Recurrent test and test after repair of medical electrical equipment
November 14, 2014 - DS

IEC 62353:2014 applies to testing of medical electrical equipment and medical electrical systems, hereafter referred to as ME equipment and ME systems, or parts of such equipment or systems, which comply with IEC 60601-1:1988 (second edition) and its...

DS/EN ISO 10524-1 - Pressure regulators for use with medical gases – Part 1: Pressure regulators and pressure regulators with flow-metering devices (ISO 10524-1:2018)
February 4, 2019 - DS

ISO 10524-1:2018 specifies the design, construction, type testing, and marking requirements for pressure regulators (as defined in 3.18) intended for the administration of medical gases and their mixtures in the treatment, management, diagnostic evaluation and care of patients or for...

ISO 22610 - Surgical drapes, gowns and clean air suits, used as medical devices, for patients, clinical staff and equipment - Test method to determine the resistance to wet bacterial penetration
September 1, 2018 - ISO

This document specifies a test method, with associated test apparatus, which is used to determine the resistance of a material to the penetration of bacteria, carried by a liquid, when subjected to mechanical rubbing.

DS/IEC TR 60601-4-3 - Medical electrical equipment – Part 4-3: Guidance and interpretation – Considerations of unaddressed safety aspects in the third edition of IEC 60601-1 and proposals for new requirements
December 18, 2018 - DS

IEC TR 60601-4-3:2018 is available as IEC TR 60601-4-3:2018 RLV which contains the International Standard and its Redline version, showing all changes of the technical content compared to the previous edition.IEC TR 60601-4-3:2018 contains a series of recommendations developed by an expert working...

ASTM G121 - Standard Practice for Preparation of Contaminated Test Coupons for the Evaluation of Cleaning Agents
December 1, 2018 - ASTM

This practice describes the procedure for the preparation of single- and double-sided contaminated test coupons for the evaluation of cleaning agents. It is applicable for the evaluation of cleaning agents proposed for the cleaning of oxygen equipment, pharmaceutical manufacturing...

DS/EN IEC 62087-7 - Audio, video, and related equipment – Methods of measurement for power consumption Part 7: Computer monitors
February 18, 2019 - DS

This part of IEC 62087 specifies the determination of the power consumption of computer monitors including, but is not limited to, those with CRT, LCD, PDP or OLED technologies. Computer monitors that include touch screen functionality are included in the scope of this document. This document is...

IEC TR 60601-4-3 - Medical electrical equipment – Part 4-3: Guidance and interpretation – Considerations of unaddressed safety aspects in the third edition of IEC 60601-1 and proposals for new requirements
December 1, 2018 - IEC

This part of IEC 60601, which is a Technical Report, contains a series of recommendations developed by an expert working group of IEC subcommittee 62A in response to questions of interpretation of IEC 60601-1:2005 and related collateral standards in the IEC 60601 series. This document is primarily...

IEC TR 60601-4-3 REDLINE - Medical electrical equipment – Part 4-3: Guidance and interpretation – Considerations of unaddressed safety aspects in the third edition of IEC 60601-1 and proposals for new requirements
December 1, 2018 - IEC

This part of IEC 60601, which is a Technical Report, contains a series of recommendations developed by an expert working group of IEC subcommittee 62A in response to questions of interpretation of IEC 60601-1:2005 and related collateral standards in the IEC 60601 series. This document is primarily...

Design and Construction of Laboratory Gas Pipelines: A Practical Reference for Engineers and Professionals
March 13, 2019 - CRC

This new volume, Design and Construction of Laboratory Gas Pipelines: A Practical Reference for Engineers and Professionals, focuses on design and installation of laboratory gas pipelines. It instructs design engineers, laboratory managers, and installation technicians on how to source the...

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...

ASTM F702 - Standard Specification for Polysulfone Resin for Medical Applications
December 1, 2018 - ASTM

This specification covers polysulfone resin (poly(oxy-1, 4-phenylenesulfonyl-1,4-phenylene (dimethylmethylene)-1, 4-phenylene)) as defined in ISO 25137-1, supplied by a vendor in virgin form (pellets, powder, fabricated forms and so forth) for medical applications. This specification...

IEC 62464-1 - Magnetic resonance equipment for medical imaging – Part 1: Determination of essential image quality parameters
December 1, 2018 - IEC

This part of IEC 62464 specifies measurement procedures for the determination of many essential image quality parameters for MR EQUIPMENT. Measurement procedures as addressed in this document are suitable for - quality assessment in the ACCEPTANCE TEST, and - quality assurance in the...

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