• Live Chinese/Taiwanese voice broadcast function

• Large LCD screen design

• The standard classification of blood pressure has been clearer

• Friendly service - Braille stickers

許可證字號：衛部醫器製字第005585號 有效日期：20290112

製造廠名稱: ROSSMAX INTERNATIONAL LTD. 製造廠登記: 63022124, 製造廠品管: GMP

• ROSSMAX INTERNATIONAL LTD. is certified under Taiwan's Medical Device Quality Management Systems (QMS) guidelines, making it a domestic medical device manufacturer.
• The company conducts and passes ISO 13485 international quality system certification annually and has a well-established management team committed to quality. For the procurement of raw materials and semi-finished products, we follow the company's established procurement procedures to ensure that the materials meet the product specifications.
• To ensure the continued stability of raw materials and semi-finished products, we have established an incoming inspection procedure. This procedure follows the ANSI/ASQ Z1.4-2003 standard for sampling inspection plans, rigorously monitoring the quality of incoming materials and keeping detailed records. Additionally, we have set up a subcontractor management procedure to define the criteria for supplier selection, evaluation, and re-evaluation, with the results being documented and preserved.
• To ensure that the quality of the finished products produced and shipped from the factory meets engineering, design specifications, standards, and customer quality requirements, we have established a finished product inspection procedure. This procedure is used for product quality validation to ensure the quality and yield of shipped products.

• Identify the hazards caused by medical devices during their life cycle.
• Estimate and evaluate relevant risks.
• Control risks and monitor the effectiveness of control measures.

The products sold in Taiwan are subject to the Regulations Governing the Notification of Serious Adverse Events of Medical Devices, the Measures for the Administration of Medical Device Safety Monitoring, and the Measures for the Recycling and Disposal of Medical Devices, and the relevant post-marketing monitoring procedures for Taiwan are formulated and implemented in accordance with the procedures.