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manufacturer In this section, the expression "manufacturer" includes any person to whom the manufactured goods have been sold or otherwise disposed of.
ACT 176 - EXCISE ACT 1976
19. Drawback. |
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manufacturer "manufacturer" means a manufacturer licenced under section 4 of the Industrial Co-ordination Act 1975 [Act 156];
PU(A) 464/2003 - ENVIRONMENTAL QUALITY (CONTROL OF EMISSION FROM MOTORCYCLES) REGULATIONS 2003
2. Interpretation. |
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manufacturer "manufacturer" means a person who manufactures tobacco into a state in which it is fit for immediate consumption by smoking or otherwise and includes a subsidiary body of a body corporate that is a manufacturer;
ACT 111 - NATIONAL TOBACCO BOARD (INCORPORATION) ACT 1973
2. Interpretation. |
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manufacturer "manufacturer"- (a) in the case of kenaf, means a person who manufactures kenaf or kenaf products and includes its subsidiary body that is a manufacturer; or (b) in the case of tobacco, means a person who manufactures tobacco into a state in which it is fit for immediate consumption by smoking or otherwise and includes its subsidiary body that is a manufacturer;
ACT 692 - NATIONAL KENAF AND TOBACCO BOARD ACT 2009
2. Interpretation. |
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manufacturer "manufacturer" includes a person holding a valid licence to manufacture issued under these Regulations;
PU(A) 103/1974 - CONTROL OF SUPPLIES REGULATIONS 1974
2. Interpretation. |
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manufacturer "manufacturer" means a person who engages in the manufacture of goods; and "to manufacture" has a corresponding meaning;
ACT 64 - SALES TAX ACT 1972
2. Interpretation. |
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manufacturer "manufacturer" means- (a) a person who is responsible for- (i) the design, production, fabrication, assembly, processing, packaging and labelling of a medical device whether or not it is the person, or a subcontractor acting on the person's behalf, who carries out these operations; and (ii) assigning to the finished medical device under his own name, its intended purpose and ensuring the finished product meets the regulatory requirement; or (b) any other person who- (i) assembles, packages, processes, fully refurbishes, reprocesses or labels one or more ready-made medical devices; and (ii) assigning to the ready-made medical device under his own name, its intended purpose and ensuring the finished product meets the regulatory requirement, but shall not include the following persons: (A) any person who assembles or adapts medical devices in the market that are intended for individual patients; and (B) any person who assembles, packages or adapts medical devices in relation to which the assembling, packaging or adaptation does not change the purpose intended for the medical devices;
ACT 737 - MEDICAL DEVICE ACT 2012
2. Interpretation |
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manufacturer "manufacturer" means a person who carries on a business of assembling, producing or processing goods, and includes- (a) any person who holds himself out to the public as a manufacturer of the goods; (b) any person who affixes his brand or mark, or causes or permits his brand or mark to be affixed, to the goods; and (c) where goods are manufactured outside Malaysia and the foreign manufacturer of the goods does not have an ordinary place of business in Malaysia, a person who imports or distributes those goods;
ACT 599 - CONSUMER PROTECTION ACT 1999
3. Interpretation. |
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manufacturer "manufacturer" means a person who is engaged in any manufacturing activity;
ACT 156 - INDUSTRIAL CO-ORDINATION ACT 1975
2. Interpretation. |