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Yiwu Kebon Healthcare expands with a new facility, 4 new production lines and advanced bandage manufacturing equipment, boosting capacity by 200% to meet growing global demand for first aid kits.

The European Union continues to strengthen its requirements for medical devices. In 2026, the EU Medical Device Regulation (MDR), Regulation (EU) 2017/745, remains a key requirement for companies exporting medical devices and applicable first aid products to the European market. For manufacturers and exporters, understanding CE marking, documentation, traceability, and EUDAMED requirements is essential for building reliable and long-term business with European customers.

As the European Union’s Packaging and Packaging Waste Regulation (PPWR), Regulation (EU) 2025/40, becomes applicable from August 12, 2026, packaging requirements in the European market are entering a new phase.

More and more people are enjoying outdoor activities such as camping, hiking, fishing, and road trips. Spending time in nature is a great way to relax and explore, but unexpected situations can always happen when we are away from cities and medical facilities.