Law of Medical Devices and Supplies
Art. 30Status unknownSaudi ArabiaRegulation
Issued by Ministry of Investment (misa.gov.sa)
The manufacturer and the authorized representative shall, in relation to their
medical devices and supplies, report the following to the NCMDR:
1. Safety alerts issued by similar regulatory authorities outside the Kingdom.
2. Risks compromising the safety of the medical device or supply.
3. Completion of the Field Safety Corrective Action.
The Arabic text is the legally binding version. The English translation is provided for guidance only.
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