Resolution 737 / 1985
Chile SUBTEL QR Code & Compliance FAQ | Subtelink
These FAQs summarize key obligations under Chile’s Exempt Resolution No. 737 (2025), which amends Resolution 1985 (2017) for Short-Range Devices (SRD). Enforcement begins February 22, 2026.
General Questions
What is Resolution 737 Exenta and when does it take effect?
Published on May 22 2025, Resolution 737 amends SUBTEL Resolution 1985 to introduce a QR-based digital compliance model for SRDs. Mandatory enforcement begins February 22 2026.
Which products are affected by the new SUBTEL requirements?
The regulation covers most Short-Range Devices—including Wi-Fi, Bluetooth, LoRa, RFID, and other wireless equipment operating in Chilean SRD bands. Medical-use SRDs remain subject to traditional type-approval.
What does 'QR-based compliance' mean?
Instead of a physical SUBTEL certificate, each device package must show a QR code that links to a Spanish-language compliance webpage displaying the product’s technical and administrative data.
QR Code and Webpage Details
Where must the QR code appear and what are its specifications?
Printed on the outer product packaging, clearly visible. Minimum size 1 cm × 1 cm (borderless, high contrast). Must link directly to the model-specific compliance page via HTTPS, without redirects.
What information must the linked webpage display?
Brand, model/HVIN, product category, frequency bands, radiated power, antenna gain, manufacturer and Chilean importer/representative details, Declaration of Conformity, and reference to test reports. All content must be in Spanish and publicly accessible.
Can we link to a marketing or e-commerce page instead?
No. The QR must open a dedicated compliance page for the exact model. SUBTEL may treat redirections or mixed content as non-compliant.
Do the test reports need to be publicly viewable under the new SUBTEL QR code requirements?
No — test reports do not need to be publicly viewable on the QR-linked page. However, SUBTEL must have access to the full reports when requested for verification or market surveillance. SUBTELink provides a secure solution: manufacturers can upload test reports in a locked format accessible only to SUBTEL and verified authorities, while keeping sensitive data protected. This ensures full compliance with Chile’s new QR code and website regulation without compromising confidentiality.
Certificates and Existing Approvals
Are existing type-approval certificates still valid?
Yes, but each model must now include a QR link to its official certificate or compliance page. No new type-approval will be issued for non-medical SRDs after February 2026.
What happens if I sell products without the QR code or webpage?
SUBTEL may suspend commercialization or exhibition of the product in Chile and can require proof of compliance before re-entry to market.
Local Representation
Who can act as the local representative in Chile?
Any legally registered Chilean company authorized to receive regulatory correspondence. Most foreign manufacturers appoint iCertifi SpA as their official representative through SUBTELink.
What are the representative’s obligations?
Maintain the model’s webpage, ensure data accuracy, hold supporting documentation for 10 years, and respond to any SUBTEL inquiries.
Compliance and Implementation
What steps ensure full compliance?
- Confirm the device’s frequency bands and power limits under Resolution 1985.
- Prepare a Declaration of Conformity (Spanish).
- Assign your Chilean importer or iCertifi SpA as representative.
- Generate and verify your QR code.
Apply the QR to packaging and verify that it resolves correctly.
How long does it take to set up through SUBTELink?
Most manufacturers receive their compliant QR and live webpage within one business day after providing documentation.
References
- Resolution 737 Exenta (2025) — Biblioteca del Congreso Nacional (BCN)
- Resolution 1985 Exenta (2017) — Original SRD standard
- SUBTEL Draft QR Specifications (2024) — format and size guidelines
Ready to comply with Chile’s QR mandate?
Resumen en Español
A partir del 22 de febrero de 2026, los equipos SRD deberán mostrar un código QR mínimo de 1 cm × 1 cm en el empaque que enlace a una página pública en español con los datos del modelo, fabricante, importador/representante en Chile, Declaración de Conformidad y evidencia de ensayo. Los equipos médicos mantienen la certificación tradicional. SUBTEL podrá fiscalizar y suspender la comercialización de productos que no cumplan con estos requisitos.
Ready to meet Chile’s new QR compliance requirements?
SUBTELink can help you create your QR webpage and documentation in one business day.