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MEDICAL ELECTRICAL EQUIPMENT - PART 2-49: PARTICULAR REQUIREMENTS FOR THE SAFETY OF MULTIFUNCTION PATIENT MONITORING EQUIPMENT (IEC 60601-2-49:2006, IDT)
MS IEC 60601-2-49:2007
Status : Original
Format : PDF

This Malaysian Standard specifies the particular safety requirements of multifunction patient monitoring equipment. 
The scope of this standard is restricted to equipment having either more tha ....Read more n one applied part or more than one single function, intended for connection to a single patient.

This standard does not specify requirements for individual monitoring functions.
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MEDICAL ELECTRICAL EQUIPMENT - PART 2-50: PARTICULAR REQUIREMENTS FOR THE SAFETY OF INFANT PHOTOTHERAPY EQUIPMENT (IEC 60601-2-50:2005, IDT)
MS IEC 60601-2-50:2007
Status : Original
Format : PDF

This Malaysian Standard specifies requirements applicable to infant phototherapy equipment, which by means of visible radiation serve to reduce bilirubin in the body of infants suffering from icterus ....Read more in the first months of life. Close

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MEDICAL ELECTRICAL EQUIPMENT – PART 2-1: PARTICULAR REQUIREMENTS FOR THE SAFETY OF ELECTRON ACCELERATORS IN THE RANGE 1 MeV TO 50 MeV (IEC 60601-2-1:1998 AND ITS AMENDMENT 1:2002, IDT)
MS IEC 60601-2-1:2006
Status : Original
Format : PDF

This Malaysian Standard applies to the manufacture and some installation aspects of electron accelerators intended for radiotherapy in human medical practice, including those in which the selection an ....Read more d display of operating parameters can be controlled automatically by programmable electronic subsystems that under normal conditions and normal use, deliver a radiation beam of x-radiation and/or electron radiation having nominal energy in the range 1 MeV to 50 MeV. Close

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Medical electrical equipment - Part 2-40: Particular requirements for the safety of electromyographs and evoked response equipment (IEC 60601-2-40:1998, IDT)
MS IEC 60601-2-40:2007 (CONFIRMED:2013)
Status : 1st Confirmation
Format : PDF

This Malaysian Standard applies to electromyographs and evoked response equipment, hereinafter referred to as equipment.

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Medical electrical equipment - Part 2-37: Particular requirements for the safety of ultrasonic medical diagnostic and monitoring equipment (IEC 60601-2-37:2004, AMD. 2:2005, IDT)
MS IEC 60601-2-37:2009 (CONFIRMED:2015)
Status : 1st Confirmation
Format : PDF

In this Malaysian Standard, safety requirements additional to those in the General Standard are specified for ultrasonic diagnostic equipment. This standard does not cover ultrasonic therapeutic equip ....Read more ment; however, equipment used for the imaging of body structures by ultrasound in conjunction with therapeutic modalities is covered. Close

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MEDICAL ELECTRICAL EQUIPMENT - PART 2-35: PARTICULAR REQUIREMENTS FOR THE SAFETY OF BLANKETS, PADS AND MATTRESSES, INTENDED FOR HEATING IN MEDICAL USE (IEC 60601-2-35:1996, IDT)
MS IEC 60601-2-35:2007
Status : Original
Format : PDF

This Malaysian Standard specifies requirements for blankets, pads, and mattresses including air-flotation mattresses and forced-air systems. 
NOTE – In this Particular Standard they are refer ....Read more red to separately as BLANKETS, PADS, or MATTRESSES, but when referred to collectively the term HEATING DEVICE is used.

HEATING DEVICES are intended for medical and paramedical use.
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Medical electrical equipment - Part 2-36: Particular requirements for the safety of equipment for extracorporeally induced lithotripsy (IEC 60601-2-36:1997, IDT)
MS IEC 60601-2-36:2007 (CONFIRMED:2013)
Status : 1st Confirmation
Format : PDF

This Malaysian Standard specifies the safety requirements of equipment for extracorporeally induced lithotripsy. The applicability of this standard is limited to components directly involved in the li ....Read more thotripsy treatment, such as, but not limited to, the generator of the pressure pulse, patient support device, and their interactions with imaging and monitoring devices. Close

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MEDICAL ELECTRICAL EQUIPMENT – PART 1-8: GENERAL REQUIREMENTS FOR SAFETY - COLLATERAL STANDARD: GENERAL REQUIREMENTS, TESTS AND GUIDANCE FOR ALARM SYSTEMS IN MEDICAL ELECTRICAL EQUIPMENT AND MEDICAL ELECTRICAL SYSTEMS (IEC 60601-1-8:2005 AND ITS AMENDMENT 1:2006, IDT)
MS IEC 60601-1-8:2007
Status : Original
Format : PDF

This Malaysian Standard specifies requirements for ALARM SYSTEMS and ALARM SIGNALS in MEDICAL ELECTRICAL EQUIPMENT and MEDICAL ELECTRICAL SYSTEMS. 
It also provides guidance for the application ....Read more of ALARM SYSTEMS. Close

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Luminaires - Part 2: Particular requirements - Section 4: Portable general purpose luminaires (First revision) (IEC 60598-2-4:1997, IDT)
MS IEC 60598-2-4:2003 (CONFIRMED:2015)
Status : 1st Revision
Format : PDF

This Malaysian Standard specifies requirements for portable general purpose luminaires, other than handlamps, for use with tungsten filament, tubular fluorescent and other discharge lamps on supply vo ....Read more ltages not exceeding 250 V. Close

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Luminaires - Part 2-5: Particular requirements - Floodlights (First revision) (IEC 60598-2-5:1998, IDT)
MS IEC 60598-2-5:2006 (CONFIRMED:2015)
Status : 1st Revision
Format : PDF

This Malaysian Standard 60598 specifies requirements for floodlights for use with tungsten filament, tubular fluorescent and other discharge lamps on supply voltages not exceeding 1,000 V.

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