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

Describe your device to check whether Környezetvédelmi termékdíj, which no longer reaches electrical equipment or batteries 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
Identifies RoHS, WEEE/EPR, battery, recycling, and producer obligations without miscalling them safety certificates. Applies when the product, feature, component, or use is in scope.
Recorded because the opposite is widely repeated and would send a manufacturer to the wrong authority. Hungary used to charge a környezetvédelmi termékdíj on electrical and electronic equipment and on batteries alongside the waste duties, but the tax authority's own current information booklet number 48, published 23 January 2026, lists only three categories of fee-liable product: egyéb kőolajtermék, egyéb műanyagtermék and egyéb vegyipari termék. Neither electrical and electronic equipment nor batteries appears anywhere in the fee-liable scope of that booklet. The residual product-fee mechanics still described there, such as the TKORNY notification to NAV within 15 days of starting the activity under Ktdt. 10. § (1), therefore bite only if the device business also places one of those three product groups on the Hungarian market; the waste-side obligation for the device itself now runs through the extended producer responsibility register and the concession company instead.
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
Evidence is normally handled inside the medical-device registration route.
Evidence is normally handled inside the medical-device registration route.
Applies when the product, feature, component, or use is in scope.
Evidence may be required, but the matrix does not identify a generic separate certificate.
Applies when the product, feature, component, or use is in scope.
Applies when the product, feature, component, or use is in scope.
Applies when the product, feature, component, or use is in scope.
Applies when the product, feature, component, or use is in scope.
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 Hungary 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.


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