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Medical electrical equipment - Part 2-16: Particular requirements for basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment (First revision) (IEC 60601-2-16:2012, IDT)
MS IEC 60601-2-16:2017
Status : 1st Revision
Format : PDF

This Malaysian Standard applies to the basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment. 
This standard does not take into consideration ....Read more the dialysis fluid control system of Haemodialysis equipment using regeneration of dialysis fluid and central delivery systems. It does however take into consideration the specific safety requirements of such haemodialysis equipment concerning electrical safety and patient safety.

This standard specifies the minimum safety requirements for haemodialysis equipment. These devices are intended for use either by medical staff or for use by the patient or other trained personnel under the supervision of medical expertise.

This standard includes all electromedical equipment that is intended to deliver a haemodialysis, haemodiafiltration and haemofiltration treatment to a patient suffering from kidney failure
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Medical electrical equipment - Part 2-13: Particular requirements for the safety and essential performance of anaesthetic systems (IEC 60601-2-13:2003, IDT)
MS IEC 60601-2-13:2006 (CONFIRMED:2013)
Status : 1st Confirmation
Format : PDF

This Malaysian Standard specifies safety and essential performance requirements for an anaesthetic system as well as individual devices designed for use in an anaesthetic system. 

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MEDICAL ELECTRICAL EQUIPMENT – PART 2-29: PARTICULAR REQUIREMENTS FOR THE SAFETY OF RADIOTHERAPY SIMULATORS (IEC 60601-2-29:1999, IDT)
MS IEC 60601-2-29:2007
Status : Withdrawn
Format : PDF

This Malaysian Standard applies to radiotherapy simulators: 
- that use diagnostic X-Ray equipment to simulate physically a radiotherapy radiation beam, so that the treatment volume to be subje ....Read more cted to irradiation during radiotherapy can be localized, and the position and size of the radiotherapy radiation field can be confirmed;

- intended exclusively for radiotherapy simulation as a prelude to intended radiotherapy, and not for any other purpose such as general diagnostic examinations; and

- used within the environmental and electrical supply conditions specified in the technical description.
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NOT FOR SALE

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MEDICAL ELECTRICAL EQUIPMENT - PART 2-33: PARTICULAR REQUIREMENTS FOR THE SAFETY OF MAGNETIC RESONANCE EQUIPMENT FOR MEDICAL DIAGNOSTIC (IEC 60601-2-33:2002, AMD. 1:2005, IDT)
MS IEC 60601-2-33:2009
Status : 1st Confirmation
Format : PDF

This Malaysian Standard applies to MR EQUIPMENT and MR SYSTEMS. This standard does not cover the application of MR EQUIPMENT beyond the INTENDED USE.

RM 165.00

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MEDICAL ELECTRICAL EQUIPMENT – PART 2-21: PARTICULAR REQUIREMENTS FOR THE SAFETY OF INFANT RADIANT WARMERS (IEC 60601-2-21:1994 AND ITS AMENDMENT 1:1996, IDT)
MS IEC 60601-2-21:2007
Status : Original
Format : PDF

This Malaysian Standard applies to infant radiant warmers. Requirements for infant radiant warmers intended for use outside a hospital baby care environment, warmers powered by an internal electrical ....Read more power source are not included in this standard. Close

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MEDICAL ELECTRICAL EQUIPMENT - PART 2-3: PARTICULAR REQUIREMENTS FOR THE SAFETY OF SHORT-WAVE THERAPY EQUIPMENT (IEC 60601-2-3:1991 AND ITS AMENDMENT 1:1998, IDT)
MS IEC 60601-2-3:2007
Status : Original
Format : PDF

This Malaysian Standard specifies the requirements for the safety of short-wave therapy equipment hereinafter referred to as equipment having a rated output power not exceeding 500 W.

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MEDICAL ELECTRICAL EQUIPMENT - PART 2-18: PARTICULAR REQUIREMENTS FOR THE SAFETY OF ENDOSCOPIC EQUIPMENT (IEC 60601-2-18:1996 AND ITS AMENDMENT 1:2000, IDT)
MS IEC 60601-2-18:2007
Status : Original
Format : PDF

This Malaysian Standard specifies requirements for the safety of endoscopic equipment and its interconnection conditions with endoscopically-used accessories. 

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MEDICAL ELECTRICAL EQUIPMENT - PART 2-26: PARTICULAR REQUIREMENTS FOR THE SAFETY OF ELECTROENCEPHALOGRAPHS (IEC 60601-2-26:2003, IDT)
MS IEC 60601-2-26:2007
Status : Original
Format : PDF

This Malaysian Standard specifies the particular safety requirements for electro-encephalographs. The special requirements for other equipment also used in electroencephalography are not covered by th ....Read more is standard, for example, cerebral function monitors; phono-photic stimulators; ectroencephalographic telemetry; EEG data storage and retrieval; equipment particularly intended for monitoring during electro-convulsive therapy; and ambulatory electroencephalographic recorders. Close

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MEDICAL ELECTRICAL EQUIPMENT – PART 2-19: PARTICULAR REQUIREMENTS FOR SAFETY OF BABY INCUBATORS (IEC 60601-2-19:1995 AND ITS AMENDMENT 1:1996,IDT)
MS IEC 60601-2-19:2007
Status : Withdrawal with replacement
Format : PDF

This Malaysian Standard specifies safety requirements for incubators. 

NOT FOR SALE

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MEDICAL ELECTRICAL EQUIPMENT – PART 2-10: PARTICULAR REQUIREMENTS FOR THE SAFETY OF NERVE AND MUSCLE STIMULATORS (IEC 60601-2-10:1987 AND ITS AMENDMENT 1:2001, IDT)
MS IEC 60601-2-10:2007
Status : Original
Format : PDF

This Malaysian Standard specifies the requirements for safety of nerve and muscle stimulators for use in the practice of physical medicine.

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