Free · No signup · Official source links

Does my medical device need EMRC radiation practice and source licence in Jordan?

Describe your device to check whether EMRC radiation practice and source licence may apply, why, what facts are missing, and which official source to review.

2 maintained routes2 official source links

Preliminary applicability · country-specific scope

What you receive

Not just a yes or no

A route-by-route answer. Separate product certificates, dossier evidence, import documents, and facility licences stay separate.

Trigger reasoning. See which product facts matter and which missing facts prevent a reliable conclusion.

Official starting points. Open the regulator or government sources behind the maintained country matrix.

Maintained country rule

What this EMRC radiation practice and source licence check is screening

Separates product, supplier, import, facility, source-holder, and operator radiation obligations. Applies when the product, feature, component, or use is in scope.

Requirement family: Ionizing radiation and radioactive sources
Regulatory object: radiation facility source or worker
Maintained rule status: mandatory if feature
Useful product facts: X-ray or radioactive source, modality, energy, import purpose, installation site, and operator role.

Radiation Protection and Nuclear Safety and Security Law No. 43 of 2007, together with Regulation No. 8 of 2013 on the bases and conditions for granting licences and permits for radiation work, makes the Energy and Minerals Regulatory Commission the single authority that permits and licenses radiation facilities, practices, sources and radiation workers, including individual licences for each device and source. EMRC publishes the practice-specific licensing instructions in its radiation-work legislation register — among them licensing requirements for radiation practices in dental centres and clinics, the licensing and inspection guide for therapeutic radiology practice, licensing of consultancy services, and licensing requirements for radiation protection officers.

How to read the answer

Classification is only the first layer

A device may have one medical risk class and still trigger separate radio, electrical, measurement, radiation, environmental, import, or installation requirements. The checker keeps each regulatory object separate.

Product approval

A certificate or approval attached to the finished product, component, or radio host.

Dossier or import evidence

Testing can belong inside the medical dossier, while some documents apply to each shipment.

Site or operator licence

Radiation, installation, use, or measurement controls may apply to a facility or operator.

Country-specific scope

Other Jordan routes to check

Check every Jordan route →

Wireless / radio

TRC type approval (الموافقة النوعية)

Handled as an import or shipment-level obligation.

Official starting points

Use these authority pages to confirm current scope, technical rules, application routes, and transition dates. A linked source does not turn a preliminary result into an authority decision.

EMRC

radiation-work legislation and licensing instructions register

About this checker

A preliminary tool, not a regulatory determination

Describe the complete product — radio, power, measurement, radiation, battery, materials, accessories, intended use, import route, and existing approvals. The free checker maps those facts to the maintained Jordan scheme matrix and links each route to its official source.

Use the result to identify questions and official sources. Final scope can depend on exact models, modules, bands, components, claims, HS codes, import structure, installation site, and current authority interpretation.

Is this the same as medical device classification in Jordan?: No. Risk classification determines the main medical-device pathway. This checker runs after classification and looks for additional product certificates, dossier evidence, import documents, and facility or operator licences.
Does “no separate certificate” mean no testing is required?: No. Safety, EMC, performance, or other evidence can still be required inside the medical-device dossier even when there is no separate national product certificate.
Is the result an official regulatory determination?: No. It is a preliminary applicability assessment. Review the linked official source and confirm the final route with the relevant authority, certification body, importer, or regulatory professional.