INMUNOENSAYO DE QUMIOLUMINISCENCIA PARA LA DETERMINACIÓN CUANTITATIVA DE LA HORMONA TIROIDEOESTIMULA HUMANA (TIROTROPINA, TSH, Htsh) EN SUERO Y PLASMA HUMANO
Mexico·Clase I·III. Agentes de
diagnóstico·BECKMAN COULTER DE
MÉXICO, S.A. DE C.V.·Registered January 22, 2024- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. Agentes de diagnóstico
- Product Type (English)
- III. Agentes de diagnóstico
- Trade Name (Spanish)
- ACCESS TSH (3ER IS).
- Trade Name (English)
- ACCESS TSH (3ER IS).
- Analysis ID
- 0218R2024 SSA
- Registration Date
- January 22, 2024
- Name (Spanish)
- BECKMAN COULTER DE MÉXICO, S.A. DE C.V.
- Name (English)
- BECKMAN COULTER DE MÉXICO, S.A. DE C.V.
Access comprehensive regulatory information for INMUNOENSAYO DE QUMIOLUMINISCENCIA PARA LA DETERMINACIÓN CUANTITATIVA DE LA HORMONA TIROIDEOESTIMULA HUMANA (TIROTROPINA, TSH, Htsh) EN SUERO Y PLASMA HUMANO (INMUNOENSAYO DE QUMIOLUMINISCENCIA PARA LA DETERMINACIÓN CUANTITATIVA DE LA HORMONA TIROIDEOESTIMULA HUMANA (TIROTROPINA, TSH, Htsh) EN SUERO Y PLASMA HUMANO) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 0218R2024 SSA and manufactured by BECKMAN COULTER DE MÉXICO, S.A. DE C.V.. The device was registered on January 22, 2024.
This page provides complete registration details including product type (III. Agentes de diagnóstico), 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.