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ROAD VEHICLES - ELECTRICAL AND ELECTRONIC EQUIPMENT FOR A SUPPLY VOLTAGE OF 42 V - ELECTRICAL LOADS (ISO 21848:2005, IDT)
MS ISO 21848:2010
Status : Withdrawal without replacement
Format : PDF

This Malaysian Standard describes the electrical loads that can affect electrical and electronic systems and components of road vehicles for a supply voltage of 42 V, which may be used in a single or ....Read more a multiple voltage electrical system. In addition, it specifies the tests and resulting requirements, test equipment accuracy being agreed upon between the vehicle manufacturer and the supplier. It does not cover electromagnetic compatibility (EMC).
NOTE Electrical loads are independent from the mounting location.
This Standard also provides design guidance for the interaction of 42 V with other system voltages.
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FOODSTUFFS - METHODS FOR THE DETECTION OF GENETICALLY MODIFIED ORGANISMS AND DERIVED PRODUCTS - PROTEIN BASED METHODS (ISO 21572:2004, IDT)
MS ISO 21572:2005
Status : Original
Format : PDF

This Malaysian Standard provides general guidelines and performance criteria for methods for the detection and/or quantitation of specific proteins derived from genetically modified (GM) plant materia ....Read more l in a specified matrix.

These general guidelines address existing antibody based methods. Methods other than those described in annex A may also detect the protein. The same criteria as outlined in this standard generally apply.
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Non-active surgical implants - Joint replacement implants - Specific requirements for knee-joint replacement implants (ISO 21536:2007, IDT)
MS ISO 21536:2010 (CONFIRMED:2015)
Status : 1st Confirmation
Format : PDF

This Malaysian Standard provides specific requirements for knee joint replacement implants. With regard to safety, this standard specifies requirements for intended performance, design attributes, mat ....Read more erials, design evaluation, manufacture, sterilization, packaging, information supplied by the manufacturer and methods of test. Close

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Non-active surgical implants - Joint replacement implants - Specific requirements for hip-joint replacement implants (ISO 21535:2007, IDT)
MS ISO 21535:2010 (CONFIRMED:2015)
Status : 1st Confirmation
Format : PDF

This Malaysian Standard provides specific requirements for hip joint replacement implants. With regard to safety, this Malaysian Standard specifies requirements for intended performance, design attrib ....Read more utes, materials, design evaluation, manufacture, sterilization, packaging, information supplied by the manufacturer, and methods of test. Close

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Non-active surgical implants - Joint replacement implants - Particular requirements (ISO 21534:2007, IDT)
MS ISO 21534:2010 (CONFIRMED:2024)
Status : 2nd Confirmation
Format : PDF

This Malaysian Standard specifies particular requirements for total and partial joint replacement implants, artificial ligaments and bone cement, hereafter referred to as implants. For the purposes of ....Read more this Malaysian Standard, artificial ligaments and their associated fixing devices are included in the term "implant".

?It specifies requirements for intended performance, design attributes, materials, design evaluation, manufacturing, sterilization, packaging and information to be supplied by the manufacturer.

Some tests required to demonstrate conformance to this International Standard are contained in or referenced in level 3 standards.
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SAFETY OF MACHINERY - LUBRICANTS WITH INCIDENTAL PRODUCT CONTACT - HYGIENE REQUIREMENTS (ISO 21469:2006, IDT)
MS ISO 21469:2007 (CONFIRMED:2025)
Status : 1st Confirmation
Format : PDF

This Malaysian Standard specifies hygiene requirements for the formulation, manufacture, use and handling of lubricants which, during manufacture and processing, can come into incidental contact (e.g. ....Read more through heat transfer, load transmission, lubrication or the corrosion protection of machinery) with products and packaging used in the food, food-processing, cosmetics, pharmaceutical, tobacco or animal-feeding-stuffs industries. Included in this document are registration criteria that can be used to assess conformance with this Malaysian standard for lubricants with incidental product contact (see Annex B). It is not applicable to substances used as product additives or to those in direct product contact (see Annex A), but confines itself to hygiene without addressing occupational health and safety matters. Nevertheless, it is considered essential that where occupational health and safety is associated with the processes concerned it be considered along with hygiene so that measures sat Close

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System engineering - Mk II function point analysis - Counting practices manual (ISO/IEC 20968:2002, IDT)
MS ISO/IEC 20968:2006 (CONFIRMED:2015)
Status : 1st Confirmation
Format : PDF

This Malaysian Standard specifies the software domains for which Mk II FPA may be applicable, application software requirement components recognised by Mk II FPA, Basic Formulae used in Mk II FPA and ....Read more Terminology used in Mk II FPA. It also defined the process for applying the MkII FPA rules and documenting the result and interpretation of the rules for a variety of software technologies (e.g., GUI, client/server, objects, etc.) Close

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Sterilization of health care products - Dry heat - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 20857:2010, IDT)
MS ISO 20857:2011 (CONFIRMED:2024)
Status : 2nd Confirmation
Format : PDF

This Malaysian Standard specifies requirements for the development, validation and routine control of a dry heat sterilization process for medical devices.

?NOTE. Although the scope of ....Read more this International Standard is limited to medical devices, it specifies requirements and provides guidance that might be applicable to other health care products.

Although this Malaysian Standard primarily addresses dry heat sterilization, it also specifies requirements and provides guidance in relation to depyrogenation processes using dry heat.

?NOTE Dry heat is often used for the depyrogenation of equipment, components and health care products and its effectiveness has been demonstrated. The process parameters for sterilization and/or depyrogenation are time and temperature. Because the conditions for depyrogenation are typically more severe than those required for sterilization, a process that has been validated for product depyrogenation will result in product sterility without additional val
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PETROLEUM PRODUCTS - DETERMINATION OF SULFUR CONTENT OF AUTOMOTIVE FUELS - ULTRAVIOLET FLUORESCENCE METHOD (ISO 20846:2004, IDT)
MS ISO 20846:2009
Status : Original
Format : PDF

This Malaysian Standard specifies an ultraviolet (UV) fluorescence test method for the determination of the sulfur content of motor gasolines, including those containing up to 2.7 % (m/m) oxygen, and ....Read more of diesel fuels, including those containing up to 5 % (V/V) fatty acid methyl ester (FAME), having sulfur contents in the range 3 mg/kg to 500 mg/kg. Other products may be analysed and other sulfur contents may be determined according to this test method; however, no precision data for products other than automotive fuels and for results outside the specified range have been established for this standard. Halogens interfere with this detection technique at concentrations above approximately 3 500 mg/kg.

NOTE 1 Some process catalysts used in petroleum and chemical refining might be polluted when trace amounts of sulfur-bearing materials are contained in the feedstocks.

NOTE 2 This test method may be used to determine sulfur in process feeds and may also be used to control sulfur in eff
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Clinical laboratory testing and in vitro diagnostic test systems - Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices - Part 2: Evaluation of performance of antimicrobial susceptibility test devices (ISO 20776-2:2007, IDT)
MS ISO 20776-2:2010 (CONFIRMED:2015)
Status : Withdrawn
Format : PDF

This Malaysian Standard establishes acceptable performance criteria for antimicrobial susceptibility test (AST) devices that are used to determine minimum inhibitory concentrations (MIC) and/or interp ....Read more retive category determinations of susceptible, intermediate and resistant (SIR) strains of bacteria to antimicrobial agents in medical laboratories. This Malaysian Standard specifies requirements for AST devices (including diffusion test systems) and procedures for assessing performance of such devices. It defines how a performance evaluation of an AST device is to be conducted. This Malaysian Standard has been developed to guide manufacturers in the conduct of performance evaluation studies. Close

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