The EU Medical Device Regulation (EU MDR 2017/745) is continuously reshaping the regulatory system for medical related products in Europe, including first aid kits and emergency medical supplies. After entering 2026, the EU market will further refine and enforce compliance requirements, especially ......
Read MoreAs global regulations continue to evolve, CE compliance has become a critical requirement for first aid kit manufacturers supplying to European markets. Recently, Yiwu Kebon Healthcare Co., Ltd. successfully conducted its annual CE audit training, reinforcing its commitment to product safety, regula......
Read MoreAs a leading manufacturer, Yiwu Kebon Healthcare announces that our First Aid Kits have officially cleared the 2026 FDA registration, CE MDR compliance, and ISO 13485 audits, ensuring medical-grade safety for global distributors
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