The company has passed CE and ISO 13485 international certifications to ensure that product quality meets global medical industry standards and further expand the European and international markets.
The US FDA registration certification marks that Texnet products meet the strict medical standards of the US market, officially enter the North American market, and expand the international business territory.
Through the European Union's new Medical Device Regulation (MDR) certification, optimize product quality and compliance with higher standards, and further enhance competitiveness in the European market.