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Yes. We provide complete technical documentation to support our importers in completing FDA registration and listing for the US market.
Key points:
1. Full technical files - Device description, labeling and specification documents.
2. Listing support - We guide the importer through FDA establishment registration and device listing.
3. US market ready - Documents prepared in FDA-accepted English format.
4. Fast start - Start the process early with our ready-to-use dossier.
Share your US market plan with us and we will confirm exactly what documentation you need.
Contact us for more details: Send Inquiry
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