China Temporarily Bans Helium Exports: learn how the July 10, 2026 rule may disrupt MRI, ECMO, and anesthesia device supply chains, compliance, and delivery planning for global buyers.

EU MDR deadline extended for ECMO and ICU devices to 2027. Learn what Regulation (EU) 2026/1347 means for compliance, exports, procurement, and roadmap filing.

Critical care surgical technology CE certified—learn what CE marking really covers, what it does not guarantee, and how buyers can reduce compliance risk in surgical and ICU equipment sourcing.

EU MDR deadline for high-risk devices extended to 2027. Learn how Class III and implantable device makers, importers, and buyers should update compliance, PMS, and procurement plans.