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Zdrowie i gospodarka · 8.05.2001

Medical Devices; Medical Device Reporting Regulations; Technical Amendment

The Food and Drug Administration (FDA) is amending its regulations governing Medical Device Reporting (MDR) requirements. When the final regulation was last amended, the regulation published with some errors and omissions that, if uncorrected, may prove to be misleading. This document corrects those errors.

Source: Federal Register — Food and Drug AdministrationOpen original release →