Free · No signup · Real registration dataUnited Arab Emirates Medical Device Registration Cost & Timeline Planner
Describe a product to estimate its EDE pathway, government registration fee, dossier preparation time, review timeline, and likely registration steps.
31 supported marketsUp to 5 countries per runStructured outputOfficial sources and registry records
Build a multi-market registration estimate
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Include intended use, users, patient population, operating principle, contact duration, and whether the device is sterile, measuring, active, implantable, software, or an IVD.
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What sits behind the estimate
Each run searches the selected countries’ registration databases for comparable products, checks current official sources, and maps the likely class and pathway to the maintained government fee and review timeline data for that market.
- What costs are included in the registration estimate?
- The estimate uses the current government fee schedule stored for each market. It does not include testing, audits, translations, local representation, consulting, notified-body or conformity-assessment fees unless they appear explicitly in the government schedule.
- How are preparation and review time different?
- Preparation time estimates the manufacturer and regulatory team’s work to create a review-ready dossier. Review time is the published or statutory regulator benchmark. The realistic end-to-end range accounts for common preparation and review delays.
- Does the planner classify my device?
- It suggests a preliminary class and pathway using the country scheme, current official sources, and similar registration records. The final classification depends on the complete intended use, design, labeling, and applicable current rules.
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