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Does my medical device need CMI mandatory verification of measuring devices in Czech Republic?

Describe your device to check whether CMI mandatory verification of measuring devices may apply, why, what facts are missing, and which official source to review.

1 maintained routes1 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 CMI mandatory verification of measuring devices check is screening

Checks whether a clinical measuring function needs model approval or initial/periodic verification. Applies to the facility, operator, or installation rather than only the product.

Requirement family: Legal metrology
Regulatory object: device with measuring function
Maintained rule status: mandatory for use site
Useful product facts: Measured quantity, clinical decision use, units, accuracy claim, and whether the value drives treatment.

Devices with a measuring function must comply with Act No. 505/1990 Sb. (metrology; hooks: § 44(2) and § 39(5) of Act No. 375/2022 Sb.); instruments listed in Vyhláška No. 345/2002 Sb. (e.g. tonometers, blood-pressure monitors, audiometers, scales, clinical thermometers) are subject to initial and periodic mandatory verification by the Czech Metrology Institute or an authorised metrology centre before and during use (SÚKL ZP-23, část 9 'Metrologie').

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 Czech Republic routes to check

Check every Czech Republic route →

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.

The maintained country source registry does not yet map a direct authority page to this exact route. The checker will not substitute an unrelated source. Confirm the current scope with the responsible authority before relying on the result.

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 Czech Republic 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 Czech Republic?: 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.