External Thread Plastic Parts

Rayboen has officially passed the annual audit of the ISO9001 Quality Management System, confirming that the company’s quality management, standardized processes and service management fully comply with international quality standards. The annual review covered the full business process, including order management, R&D, production, quality inspection and after-sales service. With strict assessment on quality control, risk management, customer response and continuous improvement, the audit fully recognized Rayboen’s stable and reliable management capabilities. As a globally recognized quality benchmark, ISO9001 underpins Rayboen’s consistent high-standard quality philosophy. This successful annual review ensures standardized, controllable and traceable operations, guaranteeing stable product quality and reliable delivery. Moving forward, Rayboen will continue to optimize its management system, upgrade refined and scientific management, and always provide customers with trustworthy products and professional services.

April 21, 2026 — Rayboen successfully held the kick-off meeting for the ISO 13485:2016 Medical Device Quality Management System Certification Project. Attended by the company’s senior management team, department leaders and key core employees, the meeting marks a pivotal step forward for Rayboen in medical compliance, quality control and global development strategy. Key Highlights of the Meeting The meeting officially announced the full implementation of the ISO 13485:2016 international standard, aiming to establish a professional medical device quality management system that covers the entire process: design and development, procurement and supply, production and manufacturing, quality control, packaging and delivery, as well as after-sales service. The meeting clarified project goals, implementation plans, role division and schedule milestones. It emphasized taking risk management as the core, regulatory compliance as the bottom line, and quality as the top priority, integrating system requirements into daily operations in depth to ensure product safety, efficacy and traceability. The launch of this certification not only realizes a systematic upgrade of the existing quality management system, but also serves as a strategic layout for the company to deepen its footprint in the medical industry and expand global business. About ISO 13485:2016 ISO 13485:2016 is a dedicated quality management system standard for the medical device industry issued by the International Organization for Standardization (ISO). It focuses on regulatory compliance, risk management and full life cycle quality control, and is widely applicable to enterprises engaged in the design, production and service of medical devices, supporting components and consumables. This standard has become the core market access requirement and credibility benchmark for global regulatory authorities including EU MDR, US FDA QSR and China NMPA, as well as international customers worldwide. The initiation of ISO 13485:2016 certification is an important milestone in the company’s development. In the future, Rayboen will take the system establishment as an opportunity to continuously optimize processes, strictly control product quality and strengthen compliance management. The company strives to obtain the certification as soon as possible, repay customers with higher-standard products and services, and contribute to the development of the global healthcare industry.

The booming global in vitro diagnostics (IVD) industry has raised higher standards for high-precision, cleanroom-grade and compliance-based production of IVD disposable consumables. In 2026, professional global exhibitions will fully focus on IVD core consumable precision molds, micro-nano injection molding, clean manufacturing and biocompatible medical materials, becoming core platforms for mold and injection molding enterprises to grasp market trends, upgrade technologies and expand domestic and overseas customers. Core 2026 Global Professional IVD-focused Exhibitions CACLP | Mar 21–23, Xiamen, China The world’s top IVD full-industry-chain exhibition, focusing on IVD dedicated multi-cavity precision molds, injection-molded consumables (pipette tips, 96-well plates, reaction cuvettes) and medical raw materials, ideal for connecting domestic end IVD manufacturers. MedtecLIVE Stuttgart | May 05–07, Stuttgart, Germany Europe’s core medical precision manufacturing event, focusing on ultra-precision molds for microfluidic chips and thin-wall IVD consumable micro-injection molding, supporting EU market expansion and compliance adaptation. ADLM | Jul 26–30, Anaheim, USA Global top clinical diagnostics expo, featuring FDA-compliant IVD injection molding processes, durable dedicated molds and standardized lab consumables for North American business layout. Medtec China | Sep 01–03, Shanghai, China Leading domestic medical manufacturing exhibition, showcasing IVD micro-precision molds, cleanroom injection molding equipment and automated integrated production lines for compliant mass production and yield optimization. Core Industry Development Trends 1. Intelligent & Automated Production: Intelligent customized injection machines and unmanned production lines become mainstream, meeting strict requirements for batch consistency and high-efficiency mass production of IVD consumables. 2. Micro & High-precision Mold Upgrading: Miniaturized, thin-wall and microfluidic IVD products drive the iteration of micro-nano high-precision, corrosion-resistant and long-life dedicated molds. 3. Green & Compliance Manufacturing: Biocompatible and eco-friendly medical materials and low-pollution clean molding processes have become the essential threshold for global high-end order cooperation. Industry Key Takeaways IVD mold and injection molding enterprises need to focus on precision mold R&D and injection process optimization, adapt to miniaturization and compliance trends, and provide one-stop customized solutions to seize global high-quality IVD market opportunities in 2026.

Mirror polishing of injection mold refers to a process of progressive grinding and polishing to achieve a mirror finish on the mold cavity surface. It enables molded parts to feature a smooth appearance, easy demolding and extended service life. 1. Purposes and Functions Improve the appearance quality of injection molded parts: Mirror molds can directly produce transparent or high-gloss parts in one molding step without subsequent surface finishing. Reduce demolding resistance: The ultra-smooth surface lowers friction and adhesion between plastic parts and the mold. Prolong mold service life: Minimize material residue and surface wear of the mold. 2. Process Flow Rough Grinding Adopt coarse sandpaper (240～400 grit) or silicon carbide grinding wheels to remove deep machining scratches and weld marks. Medium Grinding Gradually use 600～800 grit sandpaper to flatten most surface grooves and eliminate transitional grinding traces. Fine Grinding Apply 1000～1500 grit sandpaper to further refine surface texture and prepare for formal polishing. Primary Polishing Use felt polishing wheels with polishing compound for uniform polishing at medium and low speed. Mirror Finishing Polishing Switch to wool or cotton polishing wheels with ultra-fine polishing paste, perform final polishing under low speed and high pressure until the surface presents perfect mirror reflection. 3. Polishing Tools & Consumables Sandpaper / Abrasive cloth: 240, 400, 600, 800, 1000, 1500 grit Grinding wheels / Abrasive bits: Corundum grinding wheels, diamond grinding bits Polishing wheels: Felt wheel, leather wheel, wool wheel, cotton wheel Polishing compounds: Coarse, medium and fine grade alumina, chromium oxide and cerium oxide polishing paste Power tools: Angle grinder, polishing machine, portable micro polishing pen Auxiliary equipment: Ultrasonic cleaner, protective gloves, face mask, safety goggles