As implantable medical devices shrink to millimeter scales, their power systems remain the Achilles' heel. Did you know 40% of premature device failures stem from battery depletion? This paradox of miniaturization versus energy sustainability keeps engineers awake worldwide.
When medical devices account for 23% of FDA Class I recalls in 2023, why do manufacturers still struggle with IEC 60601 compliance? The answer lies in evolving electromagnetic environments and tightening regulatory requirements. Did you know a single oversight in electrical safety testing could delay product launches by 14 months on average?
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