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

Describe your device to check whether Moldovan radio equipment technical regulation and ARCOM market access may apply, why, what facts are missing, and which official source to review.
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
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 awaiting review. These are unreviewed candidate links retained from legacy data. They must not be cited as proof that this route or requirement applies.
The ministry's index names the Reglementare tehnică on placing on the market radio equipment, and the sector regulator publishes its own government-decision register. The regulator was established as the Agenția Națională pentru Reglementare în Comunicații Electronice și Tehnologia Informației (ANRCETI) and its own history page records that it was renamed the Agenția Națională pentru Reglementare în Comunicații (ARCOM) with effect from 1 January 2026, so the current authority is ARCOM. The obligation attaches to a medical device only where the device contains a radio transmitter or receiver. The technical regulation and the ARCOM decisions were not retrieved article by article, so the binding is a candidate.
How to read the answer
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.
A certificate or approval attached to the finished product, component, or radio host.
Testing can belong inside the medical dossier, while some documents apply to each shipment.
Radiation, installation, use, or measurement controls may apply to a facility or operator.
Country-specific scope
Applies when the product, feature, component, or use is in scope.
Source association awaiting review
Evidence is normally handled inside the medical-device registration route.
Source association awaiting review
Evidence is normally handled inside the medical-device registration route.
Source association awaiting review
Applies when the product, feature, component, or use is in scope.
Source association awaiting review
Applies to the facility, operator, or installation rather than only the product.
Source association awaiting review
Applies when the product, feature, component, or use is in scope.
Source association awaiting review
Handled as an import or shipment-level obligation.
Source association reviewed
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.
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 Moldova 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.


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