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 Moldovan legal metrology — official list of measuring instruments under metrological control in Moldova?
Describe your device to check whether Moldovan legal metrology — official list of measuring instruments under metrological control may apply, why, what facts are missing, and which official source to review.
1 maintained routes3 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 Moldovan legal metrology — official list of measuring instruments under metrological control check is screening
Checks whether a clinical measuring function needs model approval or initial/periodic verification. 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
- Legal metrology
- Regulatory object
- measuring instrument
- Maintained rule status
- mandatory if feature
- Useful product facts
- Measured quantity, clinical decision use, units, accuracy claim, and whether the value drives treatment.
The ministry's index names the Reglementare tehnică on placing measuring instruments on the market and the Oficial list of measuring instruments and measurements subject to legal metrological control, and the ministry's metrology section covers the designation of legal persons in legal metrology and the fund of normative documents in legal metrology. The Institutul Național de Metrologie publishes the national metrology legislation on its own site. A medical device with a measuring function therefore engages the legal-metrology regime in addition to the AMDM registration. The instruments were not read article by article, so the binding is a candidate.
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 Moldova routes to check
Product-specific
Moldovan market-surveillance and product-conformity framework
Applies when the product, feature, component, or use is in scope.
Source association awaiting review
Electrical safety
Moldovan low-voltage electrical equipment technical regulation
Evidence is normally handled inside the medical-device registration route.
Source association awaiting review
EMC
Moldovan electromagnetic-compatibility technical regulation
Evidence is normally handled inside the medical-device registration route.
Source association awaiting review
Wireless / radio
Moldovan radio equipment technical regulation and ARCOM market access
Applies when the product, feature, component, or use is in scope.
Source association awaiting review
Radiation
ANRANR ionizing-radiation regulation
Applies to the facility, operator, or installation rather than only the product.
Source association awaiting review
Environmental / battery
Moldovan waste electrical equipment and battery regulations
Applies when the product, feature, component, or use is in scope.
Source association awaiting review
Import CoC / PVoC
AMDM entry in the State Register of medical devices
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 Moldova 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 Moldova?
- 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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