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Does my medical device need ANRT radio-equipment agrément in Morocco?

Describe your device to check whether ANRT radio-equipment agrément may apply, why, what facts are missing, and which official source to review.

1 maintained routes1 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 ANRT radio-equipment agrément check is screening

Checks Wi-Fi, Bluetooth, cellular, NFC, RFID, UWB, telemetry, and proprietary radio approval. Applies when the product, feature, component, or use is in scope.

Source association reviewed. The source association has been reviewed. This does not verify every rule, date or product-specific conclusion; read the cited provisions and their limits.

Requirement family: Radio and spectrum approval
Regulatory object: radio equipment
Maintained rule status: mandatory if feature
Useful product facts: Radio technologies, bands, power, antenna, module model, approval IDs, and host integration changes.

Décision ANRT/DG/N°16/24 du 28 joumada II 1446 (30 décembre 2024), published in Bulletin Officiel n° 7376 du 6 février 2025, requires prior agrément from the ANRT before radio equipment is manufactured, imported, marketed or held in Morocco: art. 2 states the duty and art. 3 lists the equipment caught. Art. 6(c) fixes the study fee at 500 dirhams hors taxes per item, art. 7 gives the agrément a ten-year validity, and art. 11 requires the ANRT to notify its decision within fifteen (15) working days of receipt of a complete application, with a ten-day deficiency notice that suspends the clock. Art. 15 adds a duty to display the specific absorption rate from 1 May 2025. A medical device is caught only where it contains radio transmitting or receiving equipment.

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 Morocco routes to check

Check every Morocco route →

Telecom terminal

ANRT telecommunications terminal equipment agrément

Applies when the product, feature, component, or use is in scope.

Source association reviewed

Radiation

AMSSNuR authorisation for ionizing-radiation installations and sources

Applies to the facility, operator, or installation rather than only the product.

Source association reviewed

Reviewed source associations

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.

Agence Nationale de Réglementation des Télécommunications (ANRT)

Décision ANRT/DG/N°16/24 — equipment agrément: duty, scope, fee, validity and notification period

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 Morocco scheme matrix and links each route to its maintained source associations, with reviewed, candidate and unresolved states shown separately.

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 Morocco?: 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.