Standards

Withdrawal of Malaysian Standards

WITHDRAWAL OF MALAYSIAN STANDARDS

In exercise of the powers conferred by subsection 15(1) of the Standards of Malaysia Act 1996 [Act 549], the Minister declares the application of the revised standards as listed in the Schedule to be the Malaysian Standards for the purpose of this Act.

As approved by the Minister on 8 October 2020

SCHEDULE

No.

MS No.

Year

Title

1.

MS 1157:Part 39 1991 Method of test for vulcanized rubber: Part 39: Preparation of samples and test pieces for chemical tests
2. MS 1449:Part 5 1999 Rubber - Determination of metal content by atomic absorption spectrometry: Part 5: Determination of iron content (Confirmed 2013)
3. MS 1449:Part 6 1999 Rubber - Determination of metal content by atomic absorption spectrometry: Part 6: Determination of magnesium content (Confirmed 2013)
4. MS 281:Part 1 1999 Specification for natural latex concentrate: Part 1: Methods of sampling (Third revision)
5. MS 281:Part 14 2001 Natural rubber latex concentrate: Part 14: Determination nitrogen content (Third revision) (ISO 1656:1996, MOD)
6. MS 298 1985 Methods of sampling and test for raw natural rubber (First revision)
7. MS ISO 1795 2011 Rubber, raw natural and raw synthetic - Sampling and further preparative procedures (First revision) (ISO 1795:2007, IDT)
8. MS 317 1986 Specification for evaporated preserved natural rubber latices (First revision)
9. MS ISO 247 2001 Rubber - Determination of ash (First revision) (ISO 247:1990, IDT)
10. MS ISO 1827 2008 Rubber, vulcanized or thermoplastic - Determination of shear modulus and adhesion to rigid plates - Quadruple shear methods (First revision) (ISO 1827:2007, IDT)
11. MS ISO 23529 2011 Rubber - General procedures for preparing and conditioning test pieces for physical test methods (First revision) (ISO 23529:2010, IDT)
12. MS ISO 289-1 1998 Rubber, unvulcanized - Determinations using a shearing-disc viscometer - Part 1: Determination of mooney viscosity (ISO 289-1:1994, IDT)
13. MS 1359:Part 5 1994 Test methods for technically specified raw natural rubber: Part 4: Determination of mooney viscosity
14. MS ISO 289-2 1998 Rubber, unvulcanized - Determinations using a shearing-disc viscometer - Part 2: Determination of pre- vulcanization characteristics (ISO 289-2:1994, IDT)
15. MS ISO 4649 2005 Methods of test for vulcanized rubber: Part 40/1: Determination of abrasion resistance using a rotating cylindrical drum device (First revision) (ISO 4649:2002, IDT)
16. MS ISO 4666-3 2012 Rubber, vulcanized - Determination of temperature rise and resistance to fatigue in flexometer testing - Part 3:compression flexometer (Constant- strain type) (First revision) (ISO 4666-3:2010, IDT)
17. MS ISO 36 2013 Rubber, vulcanized or thermoplastic - Determination of adhesion to textile fabrics (First revision) (ISO 36:2011, IDT)
18. MS ISO 2781 2010 Rubber, vulcanized or thermoplastic - Determination of density (First revision) (ISO 2781:2008, IDT)
19. MS ISO 6502 2002 Rubber - Guide to the use of curemeters (ISO 6502-1:2018)
20. MS ISO 48 & MS ISO 48 COR 1 2007 Rubber, vulcanized or thermoplastic - Determination of hardness (Hardness between 10 IRHD and 100 IRHD) (First revision) (ISO 48:2007, IDT)

21.

MS ISO 18517 2007 Rubber, vulcanized or thermoplastic - Hardness testing - Introduction and guide
22. MS ISO 7619-1 2013 Rubber, vulcanized or thermoplastic - Determination of indentation hardness – Durometer method (Shore hardness) (First revision) (ISO 7619- 1:2010, IDT)
23. MS ISO 7619-2 2013 Rubber, vulcanized or thermoplastic - Determination of indentation hardness - IRHD pocket meter method (First revision) (ISO 7619- 2:2010, IDT)
24. MS 22442-4 2013 Medical devices utilising animal tissues and their derivatives - Part 4: Principles for elimination and/or inactivation of transmissible spongiform encephalopathy (TSE) agents and validation assays for those processes
25. MS ISO 10993-5 2013 Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009, IDT)
26. MS ISO 10993-9 2013 Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO 10993-9:2009, IDT)
27. MS ISO 14155 2013 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2011, COR.1:2011, IDT)
28. MS ISO 10993-13 2011 Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices (First revision) (ISO 10993-13:2010, IDT)
29. MS ISO 15193 2010 In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for content and presentation of reference measurement procedures (First revision) (ISO 15193:2009, IDT) (Confirmed in 2015)
30. MS ISO 15194 2010 In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for certified reference materials and the content of supporting documentation (First revision) (ISO 15194:2009, IDT) (Confirmed in 2015)
31. MS ISO 15195 2008 Laboratory medicine - Requirements for reference measurement laboratories (ISO 15195:2003, IDT) (Confirmed in 2015)
32. MS ISO 15198 2008 Clinical laboratory medicine - In vitro diagnostic medical devices - Validation of user quality control procedures by the manufacturer (ISO 15198:2004, IDT) (Confirmed in 2015)
33. MS ISO 17511 2008 In vitro diagnostic medical devices - Measurement of quantities in biological samples - Metrological traceability of values assigned to calibrators and control material (ISO 17511:2003, IDT) (Confirmed in 2015)
34. MS ISO 17593 2010 Clinical laboratory testing and in vitro medical devices - Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapy (ISO 17593:2007, IDT) (Confirmed in 2015)
35. MS ISO 18113-1 2010 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009, IDT) (Confirmed in 2015)
36. MS ISO 18113-2 2010 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2009, IDT) (Confimed in 2015)
37. MS ISO 18113-3 2010 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009, IDT) (Confirmed in 2015)
38. MS ISO 18113-4 2010 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2009, IDT) (Confirmed in 2015)
39. MS ISO 18113-5 2010 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2009, IDT) (Confirmed in 2015)
40. MS ISO 18153 2008 In vitro diagnostic medical devices - Measurement of quantities in biological samples - Metrological traceability of values for catalytic concentration of enzymes assigned to calibrators and control materials (ISO 18153:2003, IDT) (Confirmed 2015)
41. MS ISO 20776-1 2010 Clinical laboratory testing and in vitro diagnostic test systems - Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices - Part 1: Reference method for testing the in vitro activity of antimicrobial agents against rapidly growing aerobic bacteria involved in infectious diseases (ISO 20776-1:2006, IDT) (Confirmed in 2015)
42. MS ISO 20776-2 2010 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) (Confirmed in 2015)
43. MS ISO 22442-3 2010 Medical devices utilizing animal tissues and their derivatives - Part 3: Validation of the elimination and/or inactivation of viruses and transmissible spongiform encephalopathy (TSE) agents (ISO 22442-3:2007, IDT) (Confirmed in 2015)
44. MS 2218 2009 Rubber condoms - Guidance on the use of MS 113 in the quality management of natural rubber latex condoms (ISO 16038:2005, MOD)
45. MS ISO 25841 2013 Female condoms - Requirements and test methods (ISO 25841:2011, IDT)
46. MS ISO 29942 2013 Prophylactic dams - Requirements and test methods (ISO 29942:2011, IDT)
47. MS ISO 7439 2013 Copper-bearing contraceptive intrauterine devices - Requirements and tests (ISO 7439:2011, IDT)
48. MS ISO 8009 2013 Mechanical contraceptives - Reusable natural and silicone rubber contraceptive diaphragms - Requirements and tests (ISO 8009:2004, AMD. 1:2012, IDT)
49. MS IEC 62353 2013 Medical electrical equipment - Recurrent test and test after repair of medical electrical equipment (IEC 62353:2007, IDT)
50. MS ISO 26722 2010 Water treatment equipment for haemodialysis applications and related therapies (ISO 26722:2009, IDT)
51. MS 1982 2007 Evaluation and routine testing in medical imaging departments - Part 3-5: Acceptance tests - imaging performance of computed tomography x-ray equipment (IEC 61223-3-5:2004, MOD) (Confirmed in 2013)
52. MS IEC 60336 2007 Medical electrical equipment - x-ray tube assemblies for medical diagnosis - Characteristics of focal spots) (IEC 60336:2005, IDT) (Confirmed 2013)
53. MS IEC 60522 2007 Determination of the permanent filtration of x-ray tube assemblies (IEC 60522:2003, IDT) (Confirmed in 2013)
54. MS IEC 60601-2-29 2007 Medical electrical equipment – part 2-29: Particular requirements for the safety of radiotherapy simulators (IEC 60601-2-29:1999, IDT)
55. MS IEC 60601-2-7 2007 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)
56. MS IEC 60601-2-8 2007 Medical electrical equipment – Part 2-8: Particular requirements for the safety of therapeutic X-ray equipment operating in range 10KV to 1MV (IEC 60601-2-8:1987 and its amendment 1:1997, IDT)
57. MS IEC 61217 2007 Radiotherapy equipment - Coordinates, movements and scales (IEC 61217:2000, IDT)
58. MS IEC 61223-1 2007 Evaluation and routine testing in medical imaging departments - Part 1: General aspects (IEC 61223-1:1993, IDT) (Confirmed in 2013)
59. MS IEC 61223-2-1 2007 Evaluation and routine testing in medical imaging departments - Part 2-1: Constancy tests - film processors (IEC 61223-2-1:1993, IDT)
60. MS IEC 61223-2-6 2007 Evaluation and routine testing in medical imaging departments - Part 2-6: Constancy tests - X-ray equipment for computed tomography (IEC 61223-2-6:1994, IDT)
61. MS IEC 61223-3-2 2007 Evaluation and routine testing in medical imaging departments - Part 3-2: Acceptance tests - Imaging Performance of mammographic X -ray equipment (IEC 61223-3-2:1996, MOD)
62. MS IEC 61223-3-4 2007 Evaluation and routine testing in medical imaging departments - Part 3-4: Acceptance tests - imaging performance of dental x-ray equipment (IEC 61223-3-4:2000, IDT) (Confirmed in 2013)
63. MS ISO 15225 2011 Medical devices - Quality management - Medical device nomenclature data structure (First Revision) (ISO 15225:2010, IDT)
64. MS 652 1980 Specification for pentachlorophenol for use in the preservation of timber
65. MS 696 1981 Specification for coal tar creosote for the preservation of timber
66. MS 734 1981 Specification for wood preservation by means of pressure creosoting
67. MS 836 1983 Specification for tributyltin oxide wood preservative
68. MS 835 1984 Method for the quantitative analysis of bis (tri-n-butyltin) oxide preservative formulations and treated timber: Determination of total tin
69. MS 878 1984 Specification for copper naphthenate wood preservative
70. MS 1043 1986 Method for the quantitative analysis of preservative solutions and treated timber containing pentachlorophenol and pentachlorophenol laurate
71. MS 1300 1993 Specification for tributyltin naphthenate wood preservative
72. MS 1379 1995 Method for analysis of treated wood and treating solutions by x-ray spectroscopy
73. MS 452 1976 Specification for Gloves Knitted
74. MS 308: Part X11 2002 Textiles - Tests for colour fastness - Part X11: Colour fastness to hot pressing (ISO 105-X11:1994, MOD)
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