Product approval
A certificate or approval attached to the finished product, component, or radio host.
Free · No signup · Official source linksDoes my medical device need Radio Communications (Radio Equipment) Regulations Κ.Δ.Π. 310/2016, as amended in Cyprus?
Describe your device to check whether Radio Communications (Radio Equipment) Regulations Κ.Δ.Π. 310/2016, as amended may apply, why, what facts are missing, and which official source to review.
1 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 Radio Communications (Radio Equipment) Regulations Κ.Δ.Π. 310/2016, as amended 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.
Radio equipment placed on the Cypriot market is governed by the Radio Communications (Radio Equipment) (Basic) Regulations of 2016, Κ.Δ.Π. 310/2016, made under the Radio Communications legislation and harmonising Directive 2014/53/EU, together with the first amending regulations of 2026, Κ.Δ.Π. 231/2026. The Department of Electronic Communications (Τμήμα Ηλεκτρονικών Επικοινωνιών) of the Deputy Ministry of Research, Innovation and Digital Policy publishes the basic regulation and all amending regulations together as the set in force for radio equipment. The instrument was published in the Official Gazette No. 2154 of 4 November 2016 under Part III(I). There is no Cypriot type approval; where a device has a radio function the RED conformity assessment is required in addition to the MDR route. The Cypriot text is in Greek with an unusable PDF encoding, so no article number is cited.
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.
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 Cyprus routes to check
Electrical safety
Medical electrical equipment outside the Low Voltage Directive
Evidence is normally handled inside the medical-device registration route.
Source association awaiting review
EMC
EMC Directive switched off by the more specific MDR essential requirements
Evidence is normally handled inside the medical-device registration route.
Source association awaiting review
Environmental / battery
Department of Environment extended producer responsibility for WEEE and batteries
Maintained as a mandatory pre-market route.
Source association reviewed
Metrology
Weights and Measures Service — legal metrology authority
Applies to the facility, operator, or installation rather than only the product.
Source association reviewed
Radiation
Department of Labour Inspection — ionizing radiation protection and nuclear safety
Applies to the facility, operator, or installation rather than only the product.
Source association reviewed
Laser / UV / ultrasound
Department of Labour Inspection — non-ionizing radiation in the working environment
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.
Τμήμα Ηλεκτρονικών Επικοινωνιών (Department of Electronic Communications), Deputy Ministry of Research, Innovation and Digital Policy
Radio Communications (Radio Equipment) Regulations — basic regulation Κ.Δ.Π. 310/2016 with the first amendment Κ.Δ.Π. 231/2026
Τμήμα Ηλεκτρονικών Επικοινωνιών (Department of Electronic Communications), Deputy Ministry of Research, Innovation and Digital Policy
Radio Communications (Radio Equipment) (Basic) Regulations of 2016, Κ.Δ.Π. 310/2016, Official Gazette No. 2154 of 4 November 2016
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 Cyprus 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 Cyprus?
- 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.
DJ Fang
MedTech Regulatory Expert
Need help confirming a classification or planning your registration?
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