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Zdrowie i gospodarka · 01/06/2026

FDA Classifies Rigid Sterilization Container With Electronic Monitoring as Class II Device

The FDA has classified the rigid sterilization container with electronic monitoring as a Class II device, which will provide a reasonable assurance of safety and effectiveness, and is expected to reduce regulatory burdens and enhance patients' access to innovative devices.

Source: Federal Register — Health and Human ServicesOpen original release →