MOHAP · Importer licence · Product registration
The UAE is a major Gulf hub for medical supplies, serving its own market and re-export across the region. Medical devices are regulated federally by the Ministry of Health and Prevention (MOHAP), with local health authorities (e.g. DHA in Dubai, DoH in Abu Dhabi) for facility-level matters.
The importing company in the UAE must hold the appropriate trade licence and a MOHAP medical-store/importer registration. The importer of record holds these — not the overseas supplier. SWIFTSKY provides the manufacturer and certification documentation to support product registration.
Typical documentation required from SWIFTSKY per product line:
Honest note: MOHAP product registration and importer licensing must be in place before commercial import, and some documents require legalisation/attestation. Timelines vary by product and emirate. We supply all manufacturer documentation; registration and licensing sit with the buyer.
Products must meet UAE/Emirates standards (ESMA/MoIAT framework) where applicable, in addition to MOHAP medical-device requirements. SWIFTSKY's pre-shipment inspection by SGS, BV or Intertek supports conformity evidence where required.
| Item | Rate | Notes |
|---|---|---|
| Import duty — medical devices (general) | 0–5% | GCC common tariff; many medical items 0% |
| VAT | 5% | Certain healthcare supplies are zero-rated |
| Customs / handling charges | Variable | Confirm with your clearing agent |
Rates are indicative. Verify current HS codes, zero-rating and rates with a licensed UAE customs clearing agent before importing.
We supply the full manufacturer documentation pack for your MOHAP registration. You handle the licence; we handle the supply chain.