The Medical Device Registration Holder System (MAH) has been fully implemented, bringing new opportunities to the precision components industry.
Release date:
2025-09-09
With the comprehensive and deepening implementation of the Medical Device Marketing Authorization Holder (MAH) system, innovation vitality in the medical device industry has been greatly unleashed. This system has decoupled product registration certificates from manufacturing licenses, enabling R&D institutions and individuals to focus solely on product innovation—while entrusting the production process to high-quality, certified manufacturers like Kanghong Precision, which boast robust quality management systems.
With the comprehensive and deepening implementation of the Medical Device Marketing Authorization Holder (MAH) system, innovation vitality in the medical device industry has been greatly unleashed. This system has decoupled product registration certificates from manufacturing licenses, enabling R&D institutions and individuals to focus solely on product innovation—while entrusting the production process to high-quality, certified manufacturers like Kanghong Precision, which boast robust quality management systems.
This presents a significant market opportunity for the precision components manufacturing industry. Professional precision manufacturing enterprises are no longer mere subcontractors handling incoming materials—they can now actively engage in front-end design, offering customers comprehensive OEM/ODM solutions that span from material selection and process development all the way to complete assembly. Kanghong Precision’s newly constructed 100,000-level clean workshop and Class 10,000 laboratory are specifically designed to seize this historic opportunity, with the ambition of becoming the most reliable partner for medical device companies operating under the MAH system.
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