DONGGUAN, GUANGDONG, CHINA, January 15, 2026 /EINPresswire.com/ — As global healthcare regulations tighten and patient safety becomes the cornerstone of medical ...
The EU Commission published its 170-page proposal on revisions of the Medical Device Regulation (EU) 2017/745 (MDR) and the In Vitro Diagnostic Regulation (EU) 2017/746 (IVDR) on December 16, 2025.
ReShape Lifesciences has achieved EU MDR and UKCA certifications for its medical devices, enhancing market access and ensuring safety compliance. ReShape Lifesciences announced that its Quality ...
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