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.
With the rapid growth of remote patient monitoring and digital healthcare, ECG wearable devices are becoming essential in both medical and consumer health markets. However, turning a concept into a reliable, mass-producible product requires more than just design—it demands stable ECG sensor performance, manufacturing expertise, and medical-grade quality control.
At Goceng Medical, we believe that accessible and reliable healthcare solutions should support people in every stage of daily life. Our medical consumables and electrode solutions are designed to serve a wide range of care environments, helping professionals and individuals monitor, protect, and improve health with confidence.
GOCENG MEDICAL defibrillation electrodes have been certified by MDR, and the EUDAMED database has been officially updated。