TICAREFAK is pleased to announce that first aid kit product range has successfully obtained the EU Declaration of Conformity under the Medical Device Regulation (MDR).
This certification confirms that first aid kits meet the essential safety, health, and performance requirements established by European Union regulations for medical devices. It reflects the company’s continued commitment to product quality, regulatory compliance, and international standards.
The MDR certification is a key milestone in ensuring that TICAREFAK first aid kits are manufactured and controlled under strict quality management systems, supporting their suitability for distribution within the European market and other regulated regions.
“This achievement demonstrates our dedication to maintaining the highest standards in medical safety and compliance,” Kelly said. “We will continue to strengthen our regulatory framework and expand access to reliable first aid solutions globally.”
With this certification, TICAREFAK further reinforces its position as a trusted provider of first aid and emergency preparedness products in international markets.
For partnership inquiries, distribution opportunities, please contact by phone at +86-592-5566387 or by email at enquiry@ticarehealth.com.
Kelly Jojo
TICAREFAK Medical Advisor
15+ Years in Medical Device Manufacturing and Supply Experience