Chile's Undersecretariat of Telecommunications (SUBTEL) has issued Exempt Resolution No. 2219, again amending the Technical Standard for Short Range Communication Devices issued in 2017 (Exempt Resolution No. 1985) and its subsequent modifications, in particular Exempt Resolution No. 737 of 2025. The amendment responds to industry feedback, adjusts and clarifies certain compliance requirements, gives manufacturers and importers clearer guidance and opens the certification channel for specific medical devices ahead of schedule.

Main changes

1. Simplified technical parameters. Specific power spectral density limits are removed for certain equipment categories, such as those in clauses j.1) and j.5), and some transmit power definitions are simplified to reduce compliance complexity.

2. More flexible QR labelling, a key change:

- the QR code should be printed or affixed in a visible position on the outer packaging. Where that is not feasible it may be attached directly to the device or included in the accompanying paper documents such as the manual or warranty card;

- in all cases the QR code must not interfere with other markings;

- the QR code must contain a link to a Spanish-language website whose format and content comply with the rules.

3. Transitional provisions. For devices whose certification was applied for and authorised by SUBTEL before 22 February 2026, the website linked to the QR code may publish only the certification document instead of the specific product information required by the standard, such as model and declaration of conformity, giving existing stock a compliance cushion.

4. Early activation of medical device certification. A new certification category is added for medical data acquisition devices operating in the 430-440 MHz band with an EIRP of 0.1 microwatt and using frequency hopping. The provision takes effect immediately on publication, allowing manufacturers to apply at once rather than waiting until 22 February 2026.

5. Clarifications and corrections. Wording in the provisions with deferred effect has been corrected and clarified in several places to improve readability and precision without changing the intent.

The amendment follows extensive industry feedback received in 2025, which pointed to practical difficulties in areas such as displaying QR codes on unpackaged devices under the simplified certification regime originally due to take effect on 22 February 2026. By offering alternative compliance routes the new resolution reduces the burden on companies and clears the way for innovative medical devices to reach the market earlier. It also clarifies labelling and information disclosure requirements under both the old and new certification systems, helping companies prepare in advance for a smooth transition.