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Scope 1.1 These requirements apply to ultraviolet germicidal irradiation (UVGI) equipment and systems intended for installation and use in accordance with the U.S. National Electrical Code (NEC), NFPA 70 and in accordance with the Canadian Electrical Code, Part I (CEC), CSA C22.1. These requirements cover: a) UV Germicidal Equipment – These devices emit uncontained UV energy into the…

This document provides criteria for quality assurance and quality control, evaluation of the performance and the accreditation of biological dosimetry by cytogenetic service laboratories using the dicentric assay performed with manual scoring. This document is applicable to a)    the confidentiality of personal information, for the requestor and the service laboratory, b)    the laboratory safety…

This document specifies requirements and good practice recommendations for the collection and transport of samples intended for medical laboratory examinations. This document is applicable to medical laboratories and service providers, which can be independent from the medical laboratory, involved in laboratory pre-examination processes that include the examination request, patient preparation…

This document specifies general requirements for proficiency tests that are offered to in vivo bioassay measurement facilities operating a whole-body counter (WBC) or partial body counter (PBC) for monitoring of persons. It specifies minimum requirements for proficiency testing applicable to dosimetry laboratories that have dedicated facilities for in vivo monitoring and where accreditation is…

1 Scope 1.1 Standard addresses This Standard is intended to address the safe, effective, and reliable reprocessing of reusable medical devices at each phase of the reprocessing workflow, including a) establishing a QMS for the MDRA, including i) key performance indicators; ii) policies and procedures; iii) documentation; iv) roles and responsibilities; v) management review; vi) planning…

1 Scope 1.1 Purpose This Standard specifies general requirements related to the safety of human CTOs used for transplantation, and includes quality system requirements. It includes aspects of safety for potential and actual donors and recipients, personnel, and others who might be exposed to or affected by the transplantation of CTOs. 1.2 Areas of application This Standard applies to…

This document specifies general test requirements, the test rig and equipment, the test materials and the test procedure and report for determining water endurance performance of air filter elements used in air intake filter systems for rotary machinery such as stationary gas turbines, compressors and other stationary internal combustion engines. The test evaluates water endurance performance of…

This document specifies test methods for verifying the capabilities of tyres for motorcycles. Of the test methods presented, only some can be required depending on the type of tyre to be tested. The tests are carried out in the laboratory under controlled conditions. This document includes a strength test for assessing the capability of the tyre structure, with respect to breaking energy. A…

1 Scope 1.1 This Standard covers plumbing fixtures made of stainless steel alloys and specifies requirements for materials, construction, performance, testing, and markings. Note: The term “corrosion-resisting steel” is also applied to stainless steel. 1.2 This Standard covers the following plumbing fixtures: a) bathtubs; b) bidets; c) drinking fountains and water coolers; d)…

1 Scope This clause of Part 1 is replaced by the following. This part of IEC 60335 specifies safety requirements for electrically operated commercial refrigerating appliances and ICE-MAKERS that have an incorporated motor-compressor or that are supplied in two units for assembly as a single appliance in accordance with the instructions (split system). NOTE 101 Examples of appliances that are…