Product Safety and Marketing Labels

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Sustainable green

Responsible Product

Product Safety and Marketing Labels

Responsible Product

SDGs

Responsible Product

We ensure that the design, manufacturing, quality control, and shipping of our products meet customer expectations. All products comply with relevant safety and labeling regulations in various countries, such as medical devices. We strive for continuous innovation to collaborate with customers in developing innovative and sustainable technology products. Additionally, we aim to reduce the use of organic solvents and minimize waste generation.

Display materials and Advanced Battery Material

All products comply with international regulations such as RoHS, REACH, Packaging Directive, and WEEE.

Healthcare Products

All products are 100% compliant with the international regulations of REACH.

Waterproof and breathable textiles

The manufacturing process aligns with Bluesign certification, and solvent-free adhesives are used.

Core Technology and Intellectual Property Management Sustainable Design and Innovation of Products Green Logistics Chemical Management Product Safety and Marketing Labels

Product Safety and Marketing Labels

Before the sale of any medical devices sold by BenQ Materials in various countries, it is necessary to obtain the required national regulations and certifications of the respective sales regions. Currently obtained certifications include Taiwan TFDA, EU CE, US FDA, China CFDA, and others.

Countries	Applicable Product Regulations
Malaysia	Laws of Malaysia Act 737 Medical Device Act 2012
Thailand	Medical Device Act, B.E. 2551 (2008)
Indonesia	Law on Health (Law No. 36/2009) Permenkes No. 62 Year 2017
Vietnam	DECREE on Medical Equipment Management DECREE on Amendments to the Government’s Decree 36/2016/ND-CP dated May 15, 2016 on Medical Equipment Management CIRCULAR on Recognition of Medical Device Classification Results CIRCULAR on Classification of Medical Device
Philippines	Republic Act No. 9711.《AN ACT STRENGTHENING AND RATIONALIZING THE REGULATORY CAPACITY OF THE BUREAU OF FOOD AND DRUGS (BFAD) BY ESTABLISHING ADEQUATE TESTING LABORATORIES AND FIELD OFFICES, UPGRADING ITS EQUIPMENT, AUGMENTING ITS HUMAN RESOURCE COMPLEMENT, GIVING AUTHORITY TO RETAIN ITS INCOME, RENAMING IT THE FOOD AND DRUG ADMINISTRATION (FDA), AMENDING CERTAIN SECTIONS OF REPUBLIC ACT NO. 3720, AS AMENDED, AND APPROPRIATING FUNDS THEREOF.》 Republic Act No. 3720.《AN ACT TO ENSURE THE SAFETY AND PURITY OF FOODS, DRUGS, AND COSMETICS BEING MADE AVAILABLE TO THE PUBLIC BY CREATING THE FOOD AND DRUG ADMINISTRATION WHICH SHALL ADMINISTER AND ENFORCE THE LAWS PERTAINING THERETO.》
Spain	MDR

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