PBC MDR Product

Medical display meeting European CE MDR regulatory requirements for market access. Ensures safe and reliable performance across clinical applications. Facilitates faster regulatory approval in European markets.

European MDR-certified surgical instruments meeting stringent quality, safety, and regulatory compliance requirements. Suitable for hospitals, clinics, and distributors requiring certified surgical solutions.

A comprehensive platform for implantable medical devices developed by Forerunner Medical. The technology supports applications in orthopedic, spinal, and other surgical specialties with NMPA registration and CE certification.

The CARDIO M-PLUS is a multi-channel ECG system designed for cardiac monitoring and diagnostic assessment in clinical and ambulatory settings. This device supports efficient workflow for healthcare professionals requiring flexible ECG recording capabilities across various patient care scenarios.

Breast disease treatment device designed for therapeutic management of mammary conditions. Utilizes specialized technology for non-invasive treatment and rehabilitation support. Indicated for post-treatment recovery and symptom management in breast health applications.

Custom-developed active implantable medical devices for cardiac applications including pacemakers and related systems. Manufactured according to European Medical Device Regulation and ISO 13485:2016 standards.

An implantable neuromodulation device providing dual-channel deep brain stimulation for neurological conditions. The system is registered under Chinese medical device number 20243120980.

Multi-functional wearable technology platform for capturing physiological parameters including blood pressure and other vital signs. Designed for clinical-grade accuracy with regulatory clearance across major markets.