ATELLICA TM IM HORMONA ESTIMULANTE DE LA TIROIDES 3-ULTRA
EL ENSAYO ATELLICA™ IM THYROID STIMULATING HORMONE 3‑ULTRA (TSH3‑UL) ESTÁ PREVISTO PARA USO DIAGNÓSTICO IN VITRO EN LA DETERMINACIÓN CUANTITATIVA DE LA HORMONA ESTIMULANTE DE LA TIROIDES (TSH, TIROTROPINA) EN SUERO Y PLASMA (EDTA Y HEPARINA) H
THE ATELLICA™ IM THYROID STIMULATING HORMONE 3-ULTRA (TSH3-UL) ASSAY IS INTENDED FOR IN VITRO DIAGNOSTIC USE IN THE QUANTITATIVE DETERMINATION OF THYROID-STIMULATING HORMONE (TSH, THYROTROPIN) IN SERUM AND PLASMA (EDTA AND HEPARIN) H
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- ENSAYO PARA LA DETERMINACIÓN DE LA HORMONA ESTIMULANTE DE LA TIROIDES
- Trade Name (English)
- THYROID STIMULATING HORMONE ASSAY
- Analysis ID
- 1518R2018 SSA
- Registration Date
- June 13, 2018
- Name (Spanish)
- SIEMENS HEALTHCARE DIAGNOSTICS, S. DE R.L DE C.V.
- Name (English)
- SIEMENS HEALTHCARE DIAGNOSTICS, S. DE R.L DE C.V.
Access comprehensive regulatory information for ATELLICA TM IM HORMONA ESTIMULANTE DE LA TIROIDES 3-ULTRA (ATELLICA TM IM THYROID STIMULATING HORMONE 3-ULTRA) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1518R2018 SSA and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS, S. DE R.L DE C.V.. The device was registered on June 13, 2018.
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.