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 ИАОС register of persons placing electrical and electronic equipment on the market in Bulgaria?
Describe your device to check whether ИАОС register of persons placing electrical and electronic equipment on the market may apply, why, what facts are missing, and which official source to review.
1 maintained routes1 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 ИАОС register of persons placing electrical and electronic equipment on the market check is screening
Identifies RoHS, WEEE/EPR, battery, recycling, and producer obligations without miscalling them safety certificates. 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
- Environmental and battery obligations
- Regulatory object
- producer or authorised representative
- Maintained rule status
- mandatory if feature
- Useful product facts
- Battery chemistry/capacity, electrical equipment, importer/producer role, packaging, and market date.
Наредба за излязлото от употреба електрическо и електронно оборудване (ПМС № 256 от 13.11.2013 г., ДВ, бр. 100 от 2013 г.) чл. 48(1) obliges everyone who places EEE on the Bulgarian market, including at a distance, or their authorised commercial representative, to ask to be entered in the register under чл. 45, ал. 1, т. 3 ЗУО; чл. 48(2) sets a one-month deadline running from the start of the placing-on-the-market activity and requires the filing to be made electronically on the ИАОС website, listing the name and ЕИК, the trade marks used in the country, the correspondence address, the contact person, the equipment categories and whether obligations are met individually or through a recovery organisation. чл. 49 puts the same one-month deadline on notifying changes and on asking to be struck off when the activity stops. Medical devices are named inside categories 4 and 5 of приложение № 3 (large and small appliances by external dimension), so an in-scope device is registrable, while чл. 4, т. 11 keeps out devices expected to be infective before end of life and active implantable devices. Directive 2012/19/EU Article 2(4)(g) excludes devices expected to be infective before end of life and active implantable devices; other medical devices are in scope, and Article 16 requires each Member State to keep a producer register.
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 Bulgaria routes to check
Electrical safety
MDR electrical safety in place of the Low Voltage Directive
Evidence is normally handled inside the medical-device registration route.
Source association awaiting review
EMC
MDR electromagnetic compatibility in place of the EMC Directive
Evidence is normally handled inside the medical-device registration route.
Source association awaiting review
Wireless / radio
Наредба за съществените изисквания и оценяване съответствието на радиосъоръженията
Applies when the product, feature, component, or use is in scope.
No supporting source association
Environmental / battery
Наредба за пускане на пазара на ЕЕО във връзка с ограниченията за употреба на определени опасни вещества
Evidence may be required, but the matrix does not identify a generic separate certificate.
No supporting source association
Environmental / battery
ИАОС battery and accumulator producer register
Applies when the product, feature, component, or use is in scope.
No supporting source association
Environmental / battery
Продуктова такса, avoidable through individual compliance or a recovery organisation
Applies when the product, feature, component, or use is in scope.
No supporting source association
Product-specific
ЗМИ ISO 15225 nomenclature listing for wholesale permits
Evidence is normally handled inside the medical-device registration route.
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 Bulgaria 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 Bulgaria?
- 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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