• :  
BM ENG
  • Home
  • Service
  • International Standard
  • FAQ
  • Publish
  • signin
  •  Cart ()
Search Malaysian Standard (MS)
 Advanced Search Search




Wired glass - Specification
MS 2676:2019
Status : Original
Format : PDF

This Malaysian Standard specifies the dimensional and minimum quality requirements for wired glass.
The presence of the wire mesh appears to be a strengthening component, to hold the glass fragm ....Read more ent when it breaks.
This specification for wired glass is limited to compliance on safety aspect and excluding fire resistant requirement. Close

RM 30.00

Document will be sent via email



 Add To Cart
Systems and software engineering - Lifecycle profiles for Very Small Entities (VSEs) - Guide for the development of domain specific profiles (ISO/IEC TR 29110-2-2:2016, IDT)
MS 2720:2021
Status : Original
Format : PDF

This Malaysian Standard provides a guide for developing a profile which is domain-specific for VSEs (Very Small Entities) business situation. It may be used by technical advisers, including consultant ....Read more s, to help VSEs on software process problems. It also provides a conceptual framework for standardised profile developers using the ISO/IEC 29110 series concept. Close

RM 60.00

Document will be sent via email



 Add To Cart
AC and/or DC-supplied electronic control gear for tubular fluorescent lamps -Performance requirements (Second revision) (IEC 60929:2011, AMD.1:2015, IDT)
MS IEC 60929:2019 (CONFIRMED:2024)
Status : 1st Confirmation
Format : PDF

This international Standard specifies performance requirements for electronic control gear for use on a.c. at 50 Hz or 60 Hz and/or d.c. supplies, both up to 1 000 V, with operating frequencies deviat ....Read more ing from the supply frequency, associated with fluorescent lamps as specified in IEC 60081 and IEC 60901, and other fluorescent lamps for high-frequency operation.
NOTE 1 Tests in this standard are type tests. Requirements for testing individual control gear during production are not included.
NOTE 2 There are regional standards regarding the regulation of mains current harmonics and immunity for endproducts like luminaires and independent control gear. In a luminaire, the control gear is dominant in this respect.
Control gear, together with other components, should comply with these standards.
NOTE 3 Requirements for the digital addressable lighting interface of electronic control gear are given in
IEC 62386. Close

RM 105.00

Document will be sent via email



 Add To Cart
Medical electrical equipment - Part 2-35: Particular requirements for the basic safety and essential performance of heating devices using blankets, pads or mattresses and intended for heating in medical use (First revision) (IEC 80601-2-35:2009, IDT)
MS IEC 80601-2-35:2018
Status : 1st Revision
Format : PDF

This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of
HEATING DEVICES using BLANKETS, PADS or MATTRESSES in medical use, also referred to as
ME EQUIPMENT. HE ....Read more ATING DEVICES intended to prewarm a bed are included in the scope of this
International Standard.
If a clause or subclause is specifically 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.
If a clause or subclause is specifically intended to apply to a specifically defined type of ME
EQUIPMENT, as is the case with FORCED AIR DEVICES, then the clause or subclause is entitled as
such. Clauses or subclauses that apply to all types of ME EQUIPMENT within the scope of this
standard are not specifically entitled.
HAZARDS inherent in the intended physiological function of ME EQUIPMENT or ME SYSTEMS
within the scope of this standard are not covered by specific requirements in this standard
except in 7.2.13 and 8.4.1 of the general standard.
NOTE See also 4.2 of the general standard.
This particular standard does not apply to:
– HEATING DEVICES intended for physiotherapy;
– radiant warmers; for information, see IEC 60601-2-21 [12]2;
– incubators; for information, see IEC 60601-2-19 [10];
– transport incubators, for information, see IEC 60601-2-20 [11];
– cooling devices Close

RM 105.00

Document will be sent via email



 Add To Cart
Medical electrical equipmentPart 2-67: Particular requirements for basic safety and essential performance of oxygen conserving equipment (First revision) (ISO 80601-2-67:2014, IDT)
MS ISO 80601-2-67:2018
Status : 1st Revision
Format : PDF

IEC 60601-1:2005+A1:2012, 1.1 is replaced by:
This particular standard is applicable to the BASIC SAFETY and ESSENTIAL PERFORMANCE of oxygen
CONSERVING EQUIPMENT, hereafter referred to as ....Read more ME EQUIPMENT, in combination with its
ACCESSORIES intended to conserve supplemental oxygen by delivering gas intermittently and
synchronized with the PATIENT'S inspiratory cycle, when used in the HOME HEALTHCARE
ENVIRONMENT. Oxygen CONSERVING EQUIPMENT is typically used by a LAY OPERATOR.
NOTE 1 CONSERVING EQUIPMENT can also be used in professional health care facilities.
NOTE 2 CONSERVING EQUIPMENT can be used with an oxygen concentrator.
This particular standard is also applicable to those ACCESSORIES intended by their MANUFACTURER to
be connected to CONSERVING EQUIPMENT, where the characteristics of those ACCESSORIES can affect
the BASIC SAFETY or ESSENTIAL PERFORMANCE of the CONSERVING EQUIPMENT.
This particular standard is only applicable to active devices (e.g. pneumatically or electrically
powered) and is not applicable to non-active devices (e.g. reservoir cannulas).
NOTE 3 CONSERVING EQUIPMENT complying with this particular standard can be incorporated with other
devices that have their own standards, in which case the combination needs to comply with both standards.
EXAMPLES CONSERVING EQUIPMENT combined with a pressure regulator [2], an oxygen concentrator [1] or
liquid oxygen equipment [6].
If a clause or subclause is specifically 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.
HAZARDS inherent in the intended function of ME EQUIPMENT or ME SYSTEMS within the scope of this
standard are not covered by specific requirements in this standard except in 7.2.13 and 8.4.1 of the
general standard.
NOTE 4 See also 4.2 of the general standard.
This particular standard is a particular standard in the IEC 60601 series of standards. Close

RM 90.00

Document will be sent via email



 Add To Cart
Medical electrical equipment - Part 2-50: Particular requirements for the basic safety and essential performance of infant phototherapy equipment (First revision) (IEC 60601-2-50:2016, IDT)
MS IEC 60601-2-50:2018
Status : 1st Revision
Format : PDF

This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of INFANT PHOTOTHERAPY EQUIPMENT, as defined in 201.3.203 of this standard, also referred to as ME EQUIPMENT.
< ....Read more br /> If a clause or subclause is specifically 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.

HAZARDS inherent in the intended physiological function of ME EQUIPMENT or ME SYSTEMS within the scope of this standard are not covered by specific requirements in this standard except in 7.2.13 and 8.4.1 of the general standard.

NOTE See also 4.2 of the general standard.

This particular standard specifies safety requirements for INFANT PHOTOTHERAPY EQUIPMENT, but alternate methods of compliance with a specific clause by demonstrating equivalent safety will not be judged as non-compliant if the MANUFACTURER has demonstrated in his RISK MANAGEMENT FILE that the RISK presented by the HAZARD has been found to be of an acceptable level when weighed against the benefit of treatment from the device.

This particular standard does not apply to:
– devices supplying heat via BLANKETS, PADS or MATTRESSES in medical use, for information
see IEC 80601-2-35;
– INFANT INCUBATORS; for information see IEC 60601-2-19;
– INFANT TRANSPORT INCUBATORS; for information, see IEC 60601-2-20;
– INFANT RADIANT WARMERS; for information see IEC 60601-2-21. Close

RM 45.00

Document will be sent via email



 Add To Cart
Medical electrical equipment-Part 2-19: Particular requirements for the basic safety and essential performance of infant incubators (First revision) (IEC 60601-2-19:2016, IDT)
MS IEC 60601-2-19:2018
Status : 1st Revision
Format : PDF

This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of INFANT INCUBATORS, as defined in 201.3.209 of this standard, also referred to as ME EQUIPMENT.

If a ....Read more clause or subclause is specifically 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.

HAZARDS inherent in the intended physiological function of ME EQUIPMENT or ME SYSTEMS within the scope of this standard are not covered by specific requirements in this standard except in 7.2.13 and 8.4.1 of the general standard.

NOTE See also 4.2 of the general standard.

This particular standard specifies safety requirements for INFANT INCUBATORS but alternate methods of compliance with a specific clause by demonstrating equivalent safety will not be judged as non-compliant if the MANUFACTURER has demonstrated in his RISK MANAGEMENT FILE that the RISK presented by the HAZARD has been found to be of an acceptable level when weighed against the benefit of treatment from the device.

This particular standard does not apply to:

– devices supplying heat via BLANKETS, PADS or MATTRESSES in medical use; for information see IEC 80601-2-35 [3]2);
– INFANT RADIANT WARMERS; for information, see IEC 60601-2-21 [2];
– INFANT TRANSPORT INCUBATORS, for information, see IEC 60601-2-20 [1];
– INFANT PHOTOTHERAPY EQUIPMENT, for information see IEC 60601-2-50 [4] Close

RM 60.00

Document will be sent via email



 Add To Cart
FLUIDS FOR ELECTROTECHNICAL APPLICATIONS - UNUSED MINERAL INSULATING OILS FOR TRANSFORMERS AND SWITCHGEAR
MS 2322:2010
Status : Original
Format : PDF

This Malaysian Standard covers specifications and test methods for unused mineral insulating
oils. It applies to oil delivered to the agreed point and time of delivery, intended for use in
....Read more transformers, switchgear and similar electrical equipment in which oil is required as an
insulant and for heat transfer. These oils are obtained by distillation and refining of crude
petroleum. Oils with and without additives are both within the scope of this standard.
This standard is applicable only to unused mineral insulating oils. Reclaimed oils are beyond
the scope of this standard. This standard does not apply to mineral oils used as impregnants
in cables or capacitors.
NOTE. Mineral insulating oils complying with the requirements of this standard, of the same class and containing no
additives (see 3.4), are considered to be compatible with one another and can be mixed in any proportion. This does
not apply to oils containing additives. Where the user wishes to mix such oils, a check is recommended to be made to
ensure that the mixture meets the requirements of this standard. Close

RM 30.00

Document will be sent via email



 Add To Cart
RUBBER, VULCANIZED OR THERMOPLASTIC – DETERMINATION OF TENSION SET UNDER CONSTANT ELONGATION, AND OF TENSION SET, ELONGATION AND CREEP UNDER CONSTANT TENSILE LOAD (SECOND REVISION) (ISO 2285:2007, IDT)
MS ISO 2285:2007
Status : 2nd Revision
Format : PDF

This International Standard specifies a number of methods of determining the dimensional changes in test
pieces of vulcanized or thermoplastic rubber during and after tensile loading for relativ ....Read more ely short periods under
constant elongation or constant loading.
The constant-elongation test is intended to measure the ability of rubbers to retain their elastic properties after
extension, at a standard laboratory temperature, to a specified strain which is maintained for a specified time
at the same or at a specified higher temperature and then released at the test temperature or at the standard
laboratory temperature.
The constant-load test specifies a method for the determination of elongation, creep and tension set of
rubbers subjected to a constant load at standard laboratory temperature.
The test methods are intended to measure the elastic properties of rubber in the hardness range 20 IRHD to
94 IRHD.
The creep measurement is not recommended for product design or the evaluation of low-creep materials. For
these, reference should be made to ISO 8013. No agreement between the results of this test or those of
ISO 8013 should be inferred.
NOTE The constant-load test is primarily intended for the measurement of state of cure and the quality control of
thin-walled products. An increase in the state of cure or degree of crosslinking is usually reflected in a decrease in set,
creep or elongation. Close

RM 30.00

Document will be sent via email



 Add To Cart
Medical electrical equipment - Part 2-20: Particular requirements for the basic safety and essential performance of infant transport incubators (First revision) (IEC 60601-2-20:2016, IDT)
MS IEC 60601-2-20:2018
Status : 1st Revision
Format : PDF

This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of INFANT TRANSPORT INCUBATOR equipment, as defined in 201.3.211 of this standard, also referred to as ME EQUIPMENT.....Read more r />
If a clause or subclause is specifically 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. HAZARDS inherent in the intended physiological function of ME EQUIPMENT or ME SYSTEMS within the scope of this standard are not covered by specific requirements in this standard except in 7.2.13 and 8.4.1 of the general standard.

NOTE See also 4.2 of the general standard.

This particular standard specifies safety requirements for INFANT TRANSPORT INCUBATORS but alternate methods of compliance with a specific clause by demonstrating equivalent safety will not be judged as non compliant if the MANUFACTURER has demonstrated in his RISK MANAGEMENT FILE that the RISK presented by the HAZARD has been found to be of an acceptable level when weighed against the benefit of treatment from the device.

This particular standard does not apply to:

– devices supplying heat via BLANKETS, PADS or MATTRESSES in medical use; for information see IEC 80601-2-35 [1]1);
– INFANT INCUBATORS which are not INFANT TRANSPORT INCUBATOR; for information see IEC 60601-2-19 [2];
– INFANT RADIANT WARMERS; for information, see IEC 60601-2-21 [3];
– INFANT PHOTOTHERAPY; for information, see IEC 60601-2-50 [4]. Close

RM 75.00

Document will be sent via email



 Add To Cart
  • ‹
  • 1
  • 2
  • ...
  • 54
  • 55
  • 56
  • 57
  • 58
  • 59
  • 60
  • ...
  • 587
  • 588
  • ›
©2020 All rights reserved
Department of Standards Malaysia (STANDARDS MALAYSIA). Best viewed on latest browser.