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Medical device registration in Iran


We are a French distributor willing to sell medical devices (Class D) to an Iranian distributor. does the process of registration change when the supplier is himself a distributor (not a manufacturer)?
are we, as a supplier, only required to Appoint a local representative in Iran and Provide a CSDT (even if we are not the manufacturer of the medical device) ? Are we supposed to provide information on the legal manufacturer?

I appreciate your help.

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