Importing used medical equipment into Azerbaijan is legal — but compared with new equipment, it needs one additional document, and that document is often remembered only once the dossier is already under review.
Short answer: Used and refurbished medical devices can be registered and imported into Azerbaijan, provided the dossier includes the manufacturer’s document confirming the device is suitable for use, notarized and translated into Azerbaijani. Otherwise, the process is the same as for new equipment.
How does used equipment differ from new?
The core process is identical: risk classification, dossier submission to the Analytical Expertise Center (AEC), examination, and certificate issuance. The difference is one requirement — the manufacturer’s suitability-for-use document with a notarized Azerbaijani translation.
New vs. used equipment
| New | Used / refurbished | |
|---|---|---|
| Risk classification | National (Decision No. 8) | Same |
| Standard dossier | Yes | Yes |
| Manufacturer’s suitability document | Not required | Mandatory, with notarized translation |
| Class I devices | Per-batch import permit | Per-batch import permit |
What should you check before buying?
- Whether the manufacturer is still operating and can issue a suitability document.
- Whether the device’s documentation history is complete enough for translation and notarization.
- Whether the device’s risk class has been confirmed under Azerbaijani classification, not assumed from its original market.
— SME: The best time to involve us is before a used-equipment purchase, not after. One check on “can the manufacturer issue the document” can sometimes save the entire cost of the import.
Frequently asked questions
Can used medical equipment be registered in Azerbaijan?
Yes — provided the manufacturer’s suitability document is submitted with a notarized Azerbaijani translation.
What if the manufacturer no longer exists?
That makes registration significantly harder, since the mandatory document has no source. Assess this risk before buying.
Do used Class I devices need full registration?
No — like new Class I devices, a per-batch import permit is enough.
This article is for general informational purposes and does not constitute legal or regulatory advice. Requirements can change — confirm current rules, or talk to SME about your equipment.
Planning to import used medical equipment? Get in touch with SME before you buy.
Read the full overview: Medical Device Registration in Azerbaijan: Requirements, Steps, and Professional Support
Sources
Cabinet of Ministers Resolution No. 345 (18.07.2024) — e-qanun.az. Analytical Expertise Center — pharma.az.
Last reviewed: September 2026.