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 ATT homologation — terminal equipment connected to public telecommunications networks in Bolivia?
Describe your device to check whether ATT homologation — terminal equipment connected to public telecommunications networks 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 ATT homologation — terminal equipment connected to public telecommunications networks check is screening
Checks whether equipment connected to a public network needs a separate terminal-equipment route. 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
- Telecom network attachment
- Regulatory object
- terminal equipment connected to public networks
- Maintained rule status
- mandatory if feature
- Useful product facts
- Public-network connection, terminal type, cellular or wired interfaces, and network function.
The same ATT homologation regime covers terminal equipment by reference to its connection to the public network: Article 14 of Decreto Supremo N° 1391 states that homologación verifies the compatibility of operation of equipment or terminals with a telecommunications network, and Article 15.I allows the ATT to require a prototype of each equipment type for laboratory testing. The Instructivo approved by Resolución Administrativa Regulatoria ATT-DJ-RAR-TL LP 539/2024 defines 'terminal de telecomunicaciones' and 'equipo de telecomunicaciones' and requires the certificate of conformity and test reports of Article 14. Article 12 of the same instructivo makes it unlawful to advertise equipment as homologated without the certificate.
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 Bolivia routes to check
Electrical safety
AGEMED device registration dossier — quality-system certificate and technical documentation
Evidence is normally handled inside the medical-device registration route.
Source association awaiting review
Import CoC / PVoC
AGEMED imported-device dossier — consularised certificate of free sale from the origin authority
Evidence is normally handled inside the medical-device registration route.
Source association awaiting review
Wireless / radio
ATT homologation — telecommunications and ICT equipment using the radioelectric spectrum
Applies when the product, feature, component, or use is in scope.
Source association reviewed
Metrology
IBMETRO legal metrology — periodic verification of weighing instruments used in health establishments
Applies when the product, feature, component, or use is in scope.
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.
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 Bolivia 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 Bolivia?
- 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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