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High pressure sodium vapour lamps - Performance specifications (Second Revision) (IEC 60662:2011, IDT)
MS IEC 60662:2013
Status : 2nd Revision
Format : PDF

This Malaysian Standard specifies performance requirements for high-pressure sodium vapour lamps for general lighting purposes. It includes: - restriction to performance requirements - introduction of ....Read more a test device for ignition; - split of the lamp data sheets which make use of the test device and those which do not; - provisions for measurement during starting, measurement of electrical and photometrical characteristics and tests for lumen maintenance and life; - general review e.g. of maximum lamp outlines and alignment of data; - new order of data sheets by wattage. Close

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Medical electrical equipment - Part 1-2: General requirements for safety - Collateral standard electromagnetic compatibility - Requirements and test (IEC 60601-1-2:2001, IDT)
MS IEC 60601-1-2:2007 (CONFIRMED:2013)
Status : 1st Confirmation
Format : PDF

This Malaysian Standard specifies requirements and tests for electromagnetic compatibility of equipment and systems and serves as the basis of electromagnetic compatibility requirements and tests in P ....Read more articular Standards (60601-2-series). Close

RM 165.00

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Medical electrical equipment - Part 2-52: Particular requirements for the basic safety and essential performance of medical beds (IEC 60601-2-52:2009, IDT)
MS IEC 60601-2-52:2011 (CONFIRMED:2015)
Status : 1st Confirmation
Format : PDF

This Malaysian Standard applies to the basic safety and essential performance of medical beds intended for adults, hereafter referred to as medical bed.

RM 135.00

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Medical electrical equipment - Part 2-47: Particular requirements for the basic safety and essential performance of ambulatory electrocardiographic systems (First revision) (IEC 60601-2-47:2012, IDT)
MS IEC 60601-2-47:2017
Status : 1st Revision
Format : PDF

This Malaysian Standard applies the BASIC SAFETY and ESSENTIAL PERFORMANCE of AMBULATORY ELECTROCARDIOGRAPHIC SYSTEMS, hereafter referred to as ME SYSTEMS. 
If a clause or subclause is specific ....Read more ally intended to be applicable to ME EQUIPMENT only, or to ME SYSTEMS only, the title and content of that clause or subclause will say so. If that is not the case, the clause or subclause applies both to ME EQUIPMENT and to ME SYSTEMS, as relevant.

Within the scope of this standard are systems of the following types:

a) systems that provide continuous recording and continuous analysis of the ECG allowing full re-analysis giving essentially similar results. The systems may first record and store the ECG and analyse it later on a separate unit, or record and analyse the ECG simultaneously. The type of storage media used is irrelevant with regard to this standard;

b) systems that provide continuous analysis and only partial or limited recording not allowing a full re-analysis of the ECG. Close

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MEDICAL ELECTRICAL EQUIPMENT – PART 2-7: PARTICULAR REQUIREMENTS FOR THE SAFETY OF HIGH-VOLTAGE GENERATORS OF DIAGNOSTIC X-RAY GENERATORS (IEC 60601-2-7:1998, IDT)
MS IEC 60601-2-7:2007
Status : Withdrawn
Format : PDF

This Malaysian Standard applies to high-voltage generators of medical diagnostic x-ray generators and to their subassemblies including that are integrated with an x-ray tube assembly and of radiothera ....Read more py treatment simulators. Where appropriate, the requirements for x-ray generators are given but only where these concern the functioning of the associated high-voltage generators.  Close

NOT FOR SALE

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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 Close

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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. Close

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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.

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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

RM 45.00

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