KIT DE REACTIVOS PARA LA IDENTIFICACIÓN Y DIFERENCIACIÓN ESPECÍFICA DE NEISSERIA GONORRHOEAE, CHLAMYDIA TRACHOMATIS, MYCOPLASMA GENITALIUM, TRICHOMONAS VAGINALIS, UREAPLASMA UREALYTICUM, UREAPLASMA PARVUM Y/O MYCOPLASMA HOMINIS
Mexico·Clase II·III. Agentes de diagnóstico·KABLA COMERCIAL,
S.A. DE C.V.·Registered December 15, 2022- Risk Class / Clase de Riesgo
- Clase II
- Product Type (Spanish)
- III. Agentes de diagnóstico
- Product Type (English)
- III. Agentes de diagnóstico
- Trade Name (Spanish)
- VIASURE SEXUALLY TRANSMITTED DISEASES REAL TIME PCR DETECTION KIT
- Trade Name (English)
- VIASURE SEXUALLY TRANSMITTED DISEASES REAL TIME PCR DETECTION KIT
- Analysis ID
- 1614R2022 SSA
- Registration Date
- December 15, 2022
- Name (Spanish)
- KABLA COMERCIAL, S.A. DE C.V.
- Name (English)
- KABLA COMERCIAL, S.A. DE C.V.
Access comprehensive regulatory information for KIT DE REACTIVOS PARA LA IDENTIFICACIÓN Y DIFERENCIACIÓN ESPECÍFICA DE NEISSERIA GONORRHOEAE, CHLAMYDIA TRACHOMATIS, MYCOPLASMA GENITALIUM, TRICHOMONAS VAGINALIS, UREAPLASMA UREALYTICUM, UREAPLASMA PARVUM Y/O MYCOPLASMA HOMINIS (KIT DE REACTIVOS PARA LA IDENTIFICACIÓN Y DIFERENCIACIÓN ESPECÍFICA DE NEISSERIA GONORRHOEAE, CHLAMYDIA TRACHOMATIS, MYCOPLASMA GENITALIUM, TRICHOMONAS VAGINALIS, UREAPLASMA UREALYTICUM, UREAPLASMA PARVUM Y/O MYCOPLASMA HOMINIS) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1614R2022 SSA and manufactured by KABLA COMERCIAL, S.A. DE C.V.. The device was registered on December 15, 2022.
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.