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CHLAMYTOP - COFEPRIS Registration 256R2020 SSA

Access comprehensive regulatory information for CHLAMYTOP (CHLAMYTOP) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 256R2020 SSA and manufactured by PHARMACUR, S.A. DE C.V.. The device was registered on March 03, 2020.

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.

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COFEPRIS Official Data
Clase II
256R2020 SSA
CHLAMYTOP
COFEPRIS Analysis ID: 256R2020 SSA
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Product Use / Uso del Producto
Spanish

PRUEBA RรPIDA PARA LA DETECCIร“N DECLAMIDIA

English

RAPID TEST FOR THE DETECTION OF CHLAMYDIA

Device Classification
Risk Class / Clase de Riesgo
Clase II
Product Type (Spanish)
III. AGENTES DE DIAGNร“STICO
Product Type (English)
III. DIAGNOSTIC AGENTS
Trade Name (Spanish)
PRUEBA RรPIDA PARA LADETECCIร“N DE CLAMIDIA
Trade Name (English)
RAPID TEST FOR CHLAMYDIA
Registration Information
Analysis ID
256R2020 SSA
Registration Date
March 03, 2020
Manufacturer / Fabricante
Name (English)
PHARMACUR, S.A. DE C.V.