Chile QR & Website Compliance Solution
Simplifying compliance with SUBTEL’s new QR and website labeling requirements — mandatory February 2026.
Built for SUBTEL QR Compliance · Powered by iCertifi.
- Built for SUBTEL. Powered by iCertifi.
Mandatory Compliance is Here
Transform compliance from a burden to a single streamlined solution — SUBTELink manages it all.
- Built for SUBTEL. Powered by iCertifi.
Mandatory Compliance is Here
Provide secure, bilingual access to compliance documentation — automatically hosted and verified.
- Built for SUBTEL. Powered by iCertifi.
Mandatory Compliance is Here
Manage hundreds of device models with centralized QR hosting and real-time webpage updates.
- Built for SUBTEL. Powered by iCertifi.
Mandatory Compliance is Here
Launch compliant products in days, not weeks — SUBTELink accelerates market readiness.
- Built for SUBTEL. Powered by iCertifi.
Mandatory Compliance is Here
All SRDs now require QR labeling — SUBTELink keeps your compliance pages regulator-ready.
Regulatory Requirements vs iCertifi Advantage
SUBTEL Requires:
- Every SRD must display a QR code that links to a compliance webpage.
- Declaration of Conformity (DoC), certificates, and test reports must be accessible for products entering the market from February 17, 2026 onward.
- Medical SRDs require both QR + website and a type approval certificate.
SUBTELink Adds:
- Optional regulator-only access: Lock sensitive test reports so competitors cannot view them.
- Hidden, non-indexed pages: Compliance information shielded from search engines.
- Confidential hosting: DoCs, certificates, and reports stored securely.
Compliance Pathways
Existing Products (Before Feb 22, 2026):
- QR code + compliance webpage required.
- QR must link to the existing certificate PDF (view + download).
- Importer/representative information is not required.
New Products (From Feb 22, 2026):
- QR code + compliance webpage required from day one.
- Local representative required (importer, distributor, or iCertifi).
- Downloadable Declaration of Conformity (DoC).
- Test reports uploaded (locking optional via SUBTELink).
Compliance is mandatory for all SRDs in Chile. SUBTELink helps you stay ahead of enforcement.
Local Representative Requirement Simplified
SUBTEL Requirement:
- Chile’s new regulation requires all foreign manufacturers to appoint a local representative.
- The representative supports regulator communication and maintains local documentation access.
How iCertifi Helps:
- Acts as your independent Chile-based representative for SUBTEL compliance.
- Seamlessly integrated into your SUBTELink QR + website system.
- Supported by 15+ years of experience in global type approval and representation (FCC, ISED, CE, UKCA).
Why Choose SUBTELink?
Quick Answers
What is the new SUBTEL QR Code requirement in Chile?
Beginning February 21 2026, Chile’s SUBTEL will require all short-range and wireless devices, both new and existing, to include a QR code on the product, packaging, or user manual.
The QR must link to a public webpage displaying approval information, Declaration of Conformity, downloadable test reports, and the authorized local representative.
Which products must comply with the SUBTEL QR Code regulation?
Applies to SRDs, IoT equipment, and wireless transmitters (Bluetooth, Wi-Fi, Zigbee, RFID, tracking units, radar sensors).
All existing SUBTEL-approved models must also include a compliant QR code and webpage.
Telecommunication (cellular devices, gateways, routers, modules) and medical devices that use radio technologies still require formal Type Approval with SUBTEL, plus QR compliance and local representation.
When does the regulation take effect?
Mandatory on February 21 2026 (Resolución Exenta Nº 737/2025).
By that date, all products—new and existing—must have a QR code and verified webpage containing all required documentation, a direct link to the official SUBTEL certificate, and representative information.
What information must appear on the QR webpage?
- Brand and model designation
- SUBTEL certificate number + direct link to official certificate
- Declaration of Conformity (DoC)
- Downloadable test reports verifying compliance
- Authorized representative/importer in Chile
- Technical details: frequency bands, EIRP limits, standards applied
How can manufacturers or importers meet the requirement quickly?
Use SUBTELink — powered by iCertifi SpA — to generate verified webpages and QR codes within 1–2 business days.
Each page includes the certificate link, test report downloads, and local representative details.
For cellular or medical devices needing formal Type Approval, SUBTELink also manages submission + QR integration.
What happens if a product is not compliant by February 21 2026?
Non-compliant products may face import delays, restrictions, or penalties.
Early implementation prevents re-labeling costs and ensures smooth market access.
Does SUBTEL require local representation for all products?
Yes. All devices under SUBTEL jurisdiction must identify a local representative established in Chile to serve as the official point of contact.
iCertifi SpA fulfills this requirement for manufacturers using SUBTELink.
Can one QR page cover multiple models or certificates?
A single QR page may cover a model family of up to eight (8) model numbers that are technically identical and certified under identical conditions.
Each family must share the same radio parameters, frequency bands, and documentation.
Different designs or parameters require separate QR pages and certificates.
Are QR webpages hosted in Chile?
Yes. SUBTEL-compliant QR pages must be publicly accessible and hosted on secure servers ensuring availability for Chilean authorities and importers.
SUBTELink provides this infrastructure through iCertifi SpA’s verified Chilean entity, ensuring uptime and authenticity.
Which test reports does SUBTEL accept for compliance verification?
SUBTEL accepts test reports from recognized international standards, including:
- FCC (United States)
- EN / ETSI (European Union)
- ANATEL (Brazil)
Reports must demonstrate conformity with frequency bands and power limits in Resolución Exenta Nº 1985 and originate from an accredited laboratory.
Reusing valid FCC, EN, or ANATEL reports can shorten approval timelines and lower cost when the data fully represents the certified model.
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