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长寅科技股份有限公司（MedServ）成立于2016年，致力于提供医疗器材全生命周期的一站式整合服务，涵盖研发测试、技术文件撰写、质量系统辅导与全球法规支持，加速产品合规上市。我们拥有通过 ISO/IEC 17025 认证的第三方实验室，具备机械、生物、包装、灭菌与生物兼容性等多项检测能力，报告获 ILAC 国际认可。
MedServ Co., Ltd., established in 2016, provides one-stop integrated services across the entire lifecycle of medical devices. Our offerings cover R&D testing, technical documentation, quality system consulting, and global regulatory support—helping accelerate product compliance and market entry. We operate an ISO/IEC 17025-accredited third-party laboratory with capabilities in mechanical, biological, packaging, sterilization, and biocompatibility testing. All reports are internationally recognized under the ILAC MRA framework.
团队具备近20年产业经验，已协助上千件产品完成验证与注册，服务市场遍及美国、欧盟、中国、日本、东南亚与中东地区。MedServ 积极推动绿色医材与低碳医疗，协助产业制定碳管理策略，实现净零与永续发展目标。我们以「专业、诚信、效率」为核心价值，致力成为国内外医疗器材厂商在合规道路上的最佳合作伙伴。
Backed by nearly 20 years of industry experience, our team has supported the verification and registration of thousands of medical devices for markets including the United States, European Union, China, Japan, Southeast Asia, and the Middle East. MedServ is committed to advancing green medical devices and low-carbon healthcare, supporting the industry in developing carbon management strategies to achieve net-zero and long-term sustainability goals. Guided by the core values of professionalism, integrity, and efficiency, we aim to be the trusted compliance partner for medical device companies worldwide.
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