In October 2024, TÜV Rheinland LGA Products GmbH (an international independent testing, inspection, and certification body) awarded the Medical Devices Regulation (MDR) EU certificate to LargeV Instrument Coporation Limited during the 90th China International Medical Equipment Fair (CMEF).
Leveraging its innovative products and exceptional quality, LargeV successfully passed the rigorous certification process, becoming a distinguished medical equipment manufacturer to achieve MDR EU certificate.
The products that achieved MDR certificate include Smart3D series and HiRes3D series. These devices, with their advanced technology and outstanding performance, have set new benchmarks in the field of medical imaging.
LargeV's success is no coincidence—it reflects the company's relentless pursuit of product quality and continuous investment in technological innovation. Behind this achievement is a research and development team composed of professional experts, all dedicated to integrating cutting-edge technologies into products to meet the ever-evolving demands of the market.
MDR Certificate:
The “Golden Standard” of the Medical Device Industry
Medical Devices Regulation certificate is one of the strictest certifications in the European Union regarding the safety, effectiveness, and quality control of medical devices. Products that pass MDR EU certificate meet the EU's highest standards, making them eligible for sale and use across EU countries and regions. For medical device manufacturers, achieving MDR certificate serves as a powerful recognition of their product quality and corporate strength.