Importing medical devices requires different preparations depending on the nature and class of the product. The points below offer a general outline.
Preparation topics
- The product’s class and conformity with relevant legislation
- Manufacturer documents and letters of authorisation
- Company and product registrations
- Labelling and Turkish instructions for use
- Storage, transport and traceability arrangements
The advantage of planned progress
Completing documents from the start helps reduce unexpected delays during shipment. Since requirements can differ for each product, it helps to begin with a product-by-product assessment.
This article is general information, not a diagnosis or treatment recommendation. Consult a physician for a personal assessment.
