Dubai, UAE – Feb.9-12, 2026
Goceng Medical updated the ISO 13485:2016 quality management system certification successfully in the early 2025 , and continue to improve the quality and global competitiveness of medical consumables products .
We proudly announce that GOCENG MEDICAL, the legal manufacturer of the GOCENG medical devices, has been granted certification under the new MDR of the electrode pad ,disposable ECG electrode , TENS& EMS DEVICES .
GOCENG MEDICAL will continue to follow global market trends and strengthen partnerships to deliver innovative and dependable medical consumables to the international market.
Goceng Medical updated newest MDR certificates , which includes TENS ELECTRODE , DISPOSABLE ECG ELECTRODE , TENS&EMS DEVICE since June, 2024 .
Factory inspection refers to the process of examining and assessing a manufacturing facility to ensure compliance with regulations, standards, and best practices.
August 19 marks Chinese Doctors’ Day, a special day dedicated to honoring doctors and healthcare professionals for their commitment, professionalism, and contribution to protecting human health.
At GOCENG MEDICAL, we believe that reliable medical products are built not only through advanced manufacturing capabilities, but also through a dedicated and professional team.
With years of experience in medical consumables manufacturing, GOCENG MEDICAL continues to enhance its production capacity, quality management system, and service capabilities to support global customers in the healthcare industry.
Medical device companies worldwide require reliable partners who can provide customized electrode solutions according to different applications and device designs.