Tagname : clinical evaluation
![EU Extends MDR Transition to Dec]( "EU Extends MDR Transition to Dec. 2027")
EU Extends MDR Transition to Dec. 2027EU MDR transition extends to Dec. 2027 for IVD and certain imaging devices, but the Oct. 1, 2026 clinical evaluation deadline is critical. Learn how it impacts EU exports, compliance, and customs.![EU Targets MDR Annex XVI Review for Imaging Devices]( "EU Targets MDR Annex XVI Review for Imaging Devices")
EU Targets MDR Annex XVI Review for Imaging DevicesEU Targets MDR Annex XVI Review for Imaging Devices: learn how the 2027 EU deadline could impact CE certificates, supply continuity, sourcing plans, and compliance for ultrasound, X-ray, C-arm, and dental CBCT equipment.![EU MDR Annex XVI Takes Effect for Rehab Devices]( "EU MDR Annex XVI Takes Effect for Rehab Devices")
EU MDR Annex XVI Takes Effect for Rehab DevicesEU MDR Annex XVI now applies to rehab devices, moving electric wheelchairs and smart walking aids into Class IIa/IIb. See key CE, clinical evaluation, and PMPF impacts.![How to Evaluate a Medical Equipment Manufacturer for Long-Term Supply Stability]( "How to Evaluate a Medical Equipment Manufacturer for Long-Term Supply Stability")
How to Evaluate a Medical Equipment Manufacturer for Long-Term Supply StabilityMedical equipment manufacturer evaluation starts with supply stability. Learn how to assess quality, service, compliance, and parts support for dependable long-term sourcing.
