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 EKIP radio-equipment market access in Montenegro?
Describe your device to check whether EKIP radio-equipment market access may apply, why, what facts are missing, and which official source to review.
1 maintained routes2 candidate 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 EKIP radio-equipment market access 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 awaiting review. These are unreviewed candidate links retained from legacy data. They must not be cited as proof that this route or requirement applies.
- 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 Montenegrin market must meet the Pravilnik o radio opremi (Sl. list CG 127/2026, published 28.08.2026, in force 05.09.2026), the current instrument adopted under the Zakon o tehničkim zahtjevima za proizvode. It applies to a medical device only if the device contains a radio transmitter or receiver, in which case the radio equipment must be able to use the spectrum allocated to terrestrial and space radio communication without causing harmful interference; the Agency for Electronic Communications and Postal Services (EKIP) is the market-surveillance authority. A medical device that is not radio equipment carries no separate EKIP obligation.
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 Montenegro routes to check
Electrical safety
Montenegrin electrical-equipment safety requirements
Evidence is normally handled inside the medical-device registration route.
Source association awaiting review
EMC
Montenegrin electromagnetic-compatibility requirements
Evidence is normally handled inside the medical-device registration route.
Source association awaiting review
Metrology
Montenegrin legal metrology — type approval and verification of measuring instruments
Applies when the product, feature, component, or use is in scope.
Source association awaiting review
Radiation
EPA Montenegro ionizing-radiation protection
Applies to the facility, operator, or installation rather than only the product.
Source association reviewed
Laser / UV / ultrasound
Montenegrin non-ionizing radiation protection
Applies to the facility, operator, or installation rather than only the product.
Source association awaiting review
Environmental / battery
Montenegrin waste-management duties for electrical and electronic equipment
Applies when the product, feature, component, or use is in scope.
Source association awaiting review
Import CoC / PVoC
CInMED registration and unregistered-import authorisation
Handled as an import or shipment-level obligation.
Source association reviewed
Candidate sources awaiting review
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.
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 Montenegro 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 Montenegro?
- 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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