CE Certification service for medical devices under the Medical Device Directive (MDD) and Medical Device Regulation (MDR). Enables manufacturers to demonstrate compliance with EU regulatory requirements for market authorization. Includes conformity assessment, technical documentation review, and qua...
Manufactured by
INTERTEK GROUP PLC
China
Intertek is a global Total Quality Assurance provider with over 1,000 laboratories and offices in more than 100 countries. The company offers testing, inspection, certification, and assurance solutions for operational and supply chain quality assurance across industries.
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IMQ Certification (Shanghai) Co., Ltd. · China
EU MDR Certification service for medical devices ensures compliance with European Medical Device Regulation requirements. This certification validates product safety, performance, and quality management systems for market authorization in EU member states.
Applus+ Laboratories · Spain
EU Medical Device Regulation (MDR) certification service enabling manufacturers to demonstrate compliance with European regulatory requirements for medical devices. This certification validates product safety, performance, and quality standards necessary for market authorization and commercialization across EU member states.
Ente Certificazione Macchine Srl · Italy
EU Certification service for medical devices under Regulation (EU) 2017/745 (MDR). Provides comprehensive quality and safety assessment, documentation review, and regulatory compliance support to enable market authorization throughout the European Union. Essential for manufacturers seeking to demonstrate conformity with current EU medical device regulations.
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