SRS DocumentListado de exclusión — Versión 2026-2
Currentness under review. Whether this instrument remains applicable is under review. Consult the later instruments and source context below before relying on it.
Listado de productos que no requieren de registro sanitario como dispositivos médicos — Versión 2026-2 is published by Superintendencia de Regulación Sanitaria. This document is identified by its title; no separate official document code is recorded.
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Listado de productos que no requieren de registro sanitario como dispositivos médicos — Versión 2026-2
Complete 15-page SRS list marked Versión 2026-2. Its 145 numbered entries identify products that do not require registration as medical devices, subject to the corresponding product descriptions, intended-use limits and exceptions in the Detail column. The list is subject to periodic review, does not remove other applicable permit requirements, and directs questions about unlisted products to URDM through non-registration or classification requests. No issue or commencement date is printed; current applicability remains unverified.
This document is identified by its title; no separate official document code is recorded. Always confirm the current consolidated text and transition provisions with the official source before filing.