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BILIRUBIN (DIRECT) DICLOROFENILDIAZONIO BIOSYSTEMS - COFEPRIS Registration 1921R2019 SSA

Access comprehensive regulatory information for BILIRUBIN (DIRECT) DICLOROFENILDIAZONIO BIOSYSTEMS (BILIRUBIN (DIRECT) DICLOROFENILDIAZONIO BIOSYSTEMS) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1921R2019 SSA and manufactured by BIO SIMEX, S.A. DE C.V.. The device was registered on September 27, 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.

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COFEPRIS Official Data
Clase I
1921R2019 SSA
BILIRUBIN (DIRECT) DICLOROFENILDIAZONIO BIOSYSTEMS
COFEPRIS Analysis ID: 1921R2019 SSA
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Product Use / Uso del Producto
Spanish

REACTIVO PARA LA MEDICIร“N DE LA CONCENTRACIร“N DE BILIRRUBINA DIRECTA EN SUERO O PLASMA HUMANO.

English

REAGENT FOR MEASURING THE CONCENTRATION OF DIRECT BILIRUBIN IN HUMAN SERUM OR PLASMA.

Device Classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
III. AGENTES DE DIAGNร“STICO
Product Type (English)
III. DIAGNOSTIC AGENTS
Trade Name (Spanish)
REACTIVO PARA LA DETERMINACIร“N DE BILIRRUBINA DIRECTA
Trade Name (English)
REAGENT FOR THE DETERMINATION OF DIRECT BILIRUBIN
Registration Information
Analysis ID
1921R2019 SSA
Registration Date
September 27, 2019
Manufacturer / Fabricante
Name (English)
BIO SIMEX, S.A. DE C.V.