LEGIONELLA K-SET CORIS BIOCONCEPT
Mexico·Clase I·III. DIAGNOSTIC AGENTS·PHARMACUR, S.A. DE C.V.·Registered September 25, 2018PRUEBA RÁÍDA DE DIAGNÓSTICO IN VITRO PARA DETECCIÓN DE LEGIONELLA PNEUMOPHILIA LPS EN MUESTRAS DE ORINA
IN VITRO DIAGNOSTIC TEST FOR DETECTION OF LEGIONELLA PNEUMOPHILIA LPS IN URINE SAMPLES
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- PRUEBA R´´APIDA PARA LA DETECCIÓN DE LEGIONELLA PNEUMOPHILIA
- Trade Name (English)
- R ́ ́APIDA TEST FOR THE DETECTION OF LEGIONELLA PNEUMOPHILIA
- Analysis ID
- 2245R2018 SSA
- Registration Date
- September 25, 2018
- Name (Spanish)
- PHARMACUR, S.A. DE C.V.
- Name (English)
- PHARMACUR, S.A. DE C.V.
Access comprehensive regulatory information for LEGIONELLA K-SET CORIS BIOCONCEPT (LEGIONELLA K-SET CORIS BIOCONCEPT) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2245R2018 SSA and manufactured by PHARMACUR, S.A. DE C.V.. The device was registered on September 25, 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.