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3 result(s) found, displaying 1 to 3
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Cancellation or suspensionRegulatory action due to The product is not a medical device therefore the certifications made under section 41FD of the Act at the time of application are incorrect., effective 25/11/2020
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Face mask market actionProduct defect alert following review of quality, effectiveness and regulatory compliance.
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Face mask market actionProduct defect alert following review of quality, effectiveness and regulatory compliance.