Medical Devices Medical Devices services Medical Devices services Independent certification for global market access Find our servicesSearchRelevanceMedical DevicesServiceMDR Certification: EU market access for medical devices Secure EU market access and navigate Medical Device Regulation (MDR) compliance with confidence through DNV’s expert certification services and global regulatory support. Medical DevicesServiceIVDR Certification for EU Market AccessAchieve IVDR compliance and bring your IVD devices to the EU market with confidence. DNV provides expert guidance and full certification support as your trusted Notified Body.Medical DevicesServiceISO 13485 certification - Quality management for medical devicesAchieve global market access and regulatory compliance with confidence through DNV’s ISO 13485 certification services for medical device quality management systems. Medical DevicesServiceDNV Product Assurance ServicesDNV Product Assurance is a trusted Notified Body providing certification and conformity assessment services for medical products, helping customers ensure safety, drive innovation, and meet regulatory...Medical DevicesServiceTransfer your certification to DNVDNV is a designated EU Notified Body for IVDR and MDR. Transfer your certification for smoother assessments, expert guidance, and trusted compliance.Medical DevicesServiceTCP III Certification: Market Access in TaiwanAccess Taiwan’s medical device market efficiently with DNV’s TCP III certification. Our recognized audits simplify compliance by aligning EU and Taiwan regulatory standards.Medical DevicesServiceMedical Device Single Audit Program (MDSAP) – Global Market Access Streamline global market entry with DNV’s MDSAP certification; one audit covering multiple regulatory jurisdictions to help medical device manufacturers achieve faster, more efficient compliance. Medical DevicesServiceDNV MEDCERT certification servicesDNV MEDCERT is a trusted EU Notified Body for MDR. We certify medical devices for safe market access and ongoing regulatory compliance.
Medical DevicesServiceMDR Certification: EU market access for medical devices Secure EU market access and navigate Medical Device Regulation (MDR) compliance with confidence through DNV’s expert certification services and global regulatory support.
Medical DevicesServiceIVDR Certification for EU Market AccessAchieve IVDR compliance and bring your IVD devices to the EU market with confidence. DNV provides expert guidance and full certification support as your trusted Notified Body.
Medical DevicesServiceISO 13485 certification - Quality management for medical devicesAchieve global market access and regulatory compliance with confidence through DNV’s ISO 13485 certification services for medical device quality management systems.
Medical DevicesServiceDNV Product Assurance ServicesDNV Product Assurance is a trusted Notified Body providing certification and conformity assessment services for medical products, helping customers ensure safety, drive innovation, and meet regulatory...
Medical DevicesServiceTransfer your certification to DNVDNV is a designated EU Notified Body for IVDR and MDR. Transfer your certification for smoother assessments, expert guidance, and trusted compliance.
Medical DevicesServiceTCP III Certification: Market Access in TaiwanAccess Taiwan’s medical device market efficiently with DNV’s TCP III certification. Our recognized audits simplify compliance by aligning EU and Taiwan regulatory standards.
Medical DevicesServiceMedical Device Single Audit Program (MDSAP) – Global Market Access Streamline global market entry with DNV’s MDSAP certification; one audit covering multiple regulatory jurisdictions to help medical device manufacturers achieve faster, more efficient compliance.
Medical DevicesServiceDNV MEDCERT certification servicesDNV MEDCERT is a trusted EU Notified Body for MDR. We certify medical devices for safe market access and ongoing regulatory compliance.
Accelerate safe, compliant access to global medical device markets Partner with DNV to strengthen quality systems, demonstrate regulatory compliance, and build lasting confidence in the safety and performance of your medical devices worldwide. Contact our experts
