Certificación Telecom publishes the compliance page and generates the QR code that Resolution 737 requires in order to sell wireless devices in Chile. We work with manufacturers, importers, distributors and marketplace sellers, and with international compliance firms that resolve Chile through us. We analyse your test report, publish the page and hand you the print-ready QR in two business days.
Almost certainly not. Since 22 February 2026, WiFi, Bluetooth, Zigbee, RFID and IoT devices, remote controls, wireless microphones and vehicle radar no longer require a certificate from SUBTEL. What the standard requires today is that the manufacturer or importer verify compliance, publish a page with the device's data and place a QR code pointing to that page.
The word certification is now reserved for medical devices. The distinction matters: there is no filing, no docket and no certificate to wait for, but there is an obligation that SUBTEL can inspect at any time.
Todo fabricante o importador de equipos pertenecientes a cualquiera de las categorías descritas en los literales a), b), c), d), e), f), i), j) y k) del artículo 1º, antes de comercializarlos o cederlos a terceros, a cualquier título, para su uso en Chile, debe verificar que sus emisiones radioeléctricas cumplen con la totalidad de la normativa sectorial de telecomunicaciones que le sea aplicable.
Every manufacturer or importer of equipment in any of the categories described in literales a), b), c), d), e), f), i), j) and k) of article 1, before marketing it or transferring it to third parties, on any basis, for use in Chile, must verify that its radio emissions comply with all applicable sector telecommunications regulations. (Unofficial translation.)
You send us the device and its technical documentation; we resolve the rest and hand back closed compliance.
Less than most people expect. The standard asks for seven commercial fields, the technical data that comes out of the test report, and a declaration text that we supply.
We do not ask for a Chilean tax ID, incorporation deeds or corporate paperwork: Resolution 737 does not require them for the compliance page. If a provider is asking you for those as a regulatory requirement, they are not one.
We are not a lab and we do not issue test reports. What we do is read them: we extract the bands, power levels, antenna gains and modules that Section B requires, and we verify the document is usable before publishing it.
If your device has an FCC ID, in many cases we can retrieve the report from the FCC's public filings without you having to ask the manufacturer. And if the report contains confidential information, the standard allows publishing a redacted version and keeping the full one behind a password, with prior notice to SUBTEL: we handle that.
Los Informes de Ensayo o Test Reports que el fabricante o importador debe presentar, según se indica en el artículo 2°, sólo serán aceptados si provienen de laboratorios que cuenten con al menos una acreditación internacional que asegure la calidad y objetividad de sus ensayos. Las acreditaciones correspondientes deberán estar estampadas en todas las páginas del respectivo Informe de Ensayo o Test Report.
The Informes de Ensayo or Test Reports that the manufacturer or importer must present, as indicated in article 2, will only be accepted if they come from laboratories holding at least one international accreditation ensuring the quality and objectivity of their testing. The corresponding accreditations must be stamped on every page of the respective Informe de Ensayo or Test Report. (Unofficial translation.)
One practical warning: the report must come from a laboratory whose international accreditation is stamped on every page. An unaccredited in-house test by the manufacturer does not comply.
If the device holds an Oficio de Certificación from SUBTEL whose request was filed on or before 21 February 2026, publishing that Oficio is enough. It replaces all three sections: no commercial data to gather, no technical data, no declaration of conformity.
It is the cheapest and fastest case of all, and it is easy to miss. Before asking you for anything, we check whether your device falls here.
Para los equipos que hayan sido autorizados por la Subsecretaría de Telecomunicaciones mediante un Oficio de Certificación en atención a la solicitud ingresada hasta el 21 de febrero de 2026, será suficiente publicar dicha certificación en reemplazo de la información señalada en los literales A, B y C precedentes.
For equipment authorized by the Undersecretariat of Telecommunications through an Oficio de Certificación in response to a request filed on or before 21 February 2026, publishing that certification is sufficient, replacing the information indicated in literales A, B and C above. (Unofficial translation.)
Publishing the information is the manufacturer's or the importer's duty. If you are a merchant reselling a product that already carries the QR code of the brand or of its Chilean importer, that QR works and you do not need a page of your own: the standard does not ask every link in the chain to publish its own copy.
That said, the prohibition is written about display, so whoever exhibits or sells a device without a QR is the one exposed to the penalty, even when the party who can fix it is their supplier. If the product you sell does not carry a QR, the problem is yours even though the duty to publish is not. Write to us and we will tell you which case you are in.
Tell us the brand, model and technology. We will confirm which regime applies and send you a quote.
Request a quoteThe only category that still requires a SUBTEL certificate. MICS implants, medical data acquisition and other medical equipment (literales g and h).
For manufacturers with no Chilean entity. The standard requires a manufacturer, importer or representative with legal domicile in the country, with no exceptions.