FTD URETHRITIS BASIC
Mexico·Clase II·III. DIAGNOSTIC AGENTS·SIEMENS HEALTHCARE DIAGNOSTICS, S. DE R.L. DE C.V.·Registered February 14, 2019FTD URETHRITIS BASIC ES UNA PRUEBA IN VITRO PARA LA DETECCIÓN DE ÁCIDOS NUCLEICOS EN MUESTRAS DE ORINA, GENITALES E HISOPOS RECTALES DE ORIGEN HUMANO, COMO UNA AYUDA PARA LA EVALUACIÓN DE INFECCIONES POR CHLAMYDIA TRACHOMATIS, NEISSERIA GONORRHOEAE Y MYCO
FTD URETHRITIS BASIC IS AN IN VITRO TEST FOR THE DETECTION OF NUCLEIC ACIDS IN URINE, GENITAL, AND RECTAL SWABS OF HUMAN ORIGIN, AS AN AID TO THE EVALUATION OF CHLAMYDIA TRACHOMATIS, NEISSERIA GONORRHOEAE AND MYCO INFECTIONS.
- Risk Class / Clase de Riesgo
- Clase II
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- ENSAYO PARA LA DETERMINACIÓN DE ÁCIDOS NUCLEICOS
- Trade Name (English)
- NUCLEIC ACID ASSAY
- Analysis ID
- 279R2019 SSA
- Registration Date
- February 14, 2019
- 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 FTD URETHRITIS BASIC (FTD URETHRITIS BASIC) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 279R2019 SSA and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS, S. DE R.L. DE C.V.. The device was registered on February 14, 2019.
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.