CONSULENTE DOGANALE:Da un’indagine condotta sul sito dell’Agenzia delle Dogane non risulta che attualmente il prodotto sia soggetto a restrizioni particolari per cui è di libera esportazione (senza autorizzazioni particolari)

Dal punto di vista dei pagamenti, trattandosi di attrezzature mediche, è prevista una specifica facilitazione che permette il pagamento con la sola notifica preventiva che effettuerà per vostro conto la banca (quindi non appare necessaria, l’autorizzazione che di norma è richiesta, anche se il vostro importo supera i 40.000 euro).
Certificate of Good Manufacturing Practice: A document certifying that manufacturing sites of foodstuffs, pharmaceutical products or medical devices and their manufacturing methods comply with the requirements of Good Manufacturing Practice (GMP). The certificate is to be issued by the competent authority of the country of origin. The Iranian authorities accept certificates issued by the competent authority of any EU member state if all relevant information is provided. No specific form required. The certificate is to contain the details shown in the model below. It may be prepared in any language. However, a translation into Persian or English is recommendable
Declaration of Conformity: The declaration is to be prepared by the manufacturer of the goods on a company letterhead. In specific, it must include the applicable norms to which the products conform.The certificate may be prepared in any language. A translation into Persian or English may, however, be required
Declaration of Conformity for Medical Devices: The declaration is to be completed by the manufacturer of the devices on a company letterhead in accordance with the model form provided by the Medical Equipment Department. The declaration is to be prepared in English. To be submitted in one copy.
Verification of Conformity: A document certifying the customs classification and the customs value of goods to be imported as well as their adherence to Iranian standards and norms on a mandatory basis
Registration of Medical Devices: The importer and distributor of medical devices must be officially registered as an agent of the foreign manufacturer.
Per molti di questi aspetti è opportuno sentire una delle società di sorveglianza tra: SGS, Bureau Veritas, Cotecna o InterTek