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Does my medical device need Radio equipment conformity assessment under Dz.U. 2016 poz. 878 in Poland?

Describe your device to check whether Radio equipment conformity assessment under Dz.U. 2016 poz. 878 may apply, why, what facts are missing, and which official source to review.

7 maintained routes11 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 Radio equipment conformity assessment under Dz.U. 2016 poz. 878 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.

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.

The rozporządzenie of the Minister of Digital Affairs of 17 June 2016 transposes Directive 2014/53/EU under the conformity-assessment and market-surveillance act of 13 April 2016. §2 requires radio equipment placed on the market or put into service to meet the statutory essential requirements, §3 lists the three RED routes — internal production control, EU type examination with conformity to type, and full quality assurance — and §4(3) has the manufacturer affix the CE marking. The Prezes UKE conducts product checks under art. 58(2)(3) of the act. No national type approval appears in the instrument, though this is an absence finding rather than an express negative, and a 2026 consolidated text exists whose cross-references may have moved.

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 Poland routes to check

Check every Poland route →

Electrical safety

MDR electrical safety in place of the Low Voltage Directive

Evidence is normally handled inside the medical-device registration route.

EMC

MDR electromagnetic compatibility in place of the EMC Directive

Evidence is normally handled inside the medical-device registration route.

Environmental / battery

RoHS essential requirements under Dz.U. 2021 poz. 1513

Evidence may be required, but the matrix does not identify a generic separate certificate.

Environmental / battery

BDO register entry before starting the activity

Maintained as a mandatory pre-market route.

Environmental / battery

Battery producers in the same BDO register

Maintained as a mandatory pre-market route.

Radiation

Prawo atomowe zezwolenie for radiation activity

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

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.

Sejm Rzeczypospolitej Polskiej (ELI)

Dz.U. 2016 poz. 878 §§ 2-4 — radio equipment conformity assessment and CE marking

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 Poland 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 Poland?: 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.