ST AIA-PACK TT3 - COFEPRIS Registration 1334R2021 SSA
Access comprehensive regulatory information for ST AIA-PACK TT3 (ST AIA-PACK TT3) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1334R2021 SSA and manufactured by DICIPA, S.A. DE C.V.. The device was registered on March 09, 2021.
This page provides complete registration details including product type (III. DIAGNOSTIC AGENTS), manufacturer information, and regulatory compliance data from the official Mexico COFEPRIS medical device database. Pure Global AI offers free access to Mexico's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate COFEPRIS regulations efficiently.
ST AIA-PACK TT3 ESTÁ DISEÑADO PARA SUUSOSOLAMENTEENDIAGNÓSTICOINVITROPARA LA MEDICIÓN CUANTITATIVA DECUANTITATIVA DE TRIYODOTIRONINA TOTAL(TT3) EN SUERO O PLASMA HEPARINIZADOHUMANO EN LOS ANALIZADORESESPECÍFICOS DEL SISTEMA AIA DE TOSOH.
ST AIA-PACK TT3 IS DESIGNED TO SUPPOSE ONLY IN DIAGNOSTIC USE FOR QUANTITATIVE MEASUREMENT OF TOTAL TRIIODOTHYRONINE (TT3) IN HUMAN SERUM OR HEPARINISED PLASMA IN THE SPECIFIC ANALYZERS OF THE TOSOH AIA SYSTEM.