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ALINITY I C-PEPTIDE - COFEPRIS Registration 635R2019 SSA

Access comprehensive regulatory information for ALINITY I C-PEPTIDE (ALINITY I C-PEPTIDE) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 635R2019 SSA and manufactured by ABBOTT LABORATORIES DE MEXICO SA DE CV. The device was registered on March 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 II
635R2019 SSA
ALINITY I C-PEPTIDE
COFEPRIS Analysis ID: 635R2019 SSA
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Product Use / Uso del Producto
Spanish

ENSAYO PARA LA DETERMINACIร“N DE Pร‰PTIDO C.

English

TEST FOR THE DETERMINATION OF PEPTIDE C.

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)
ENSAYO PARA LA DETERMINACIร“N DE Pร‰PTIDO C.
Trade Name (English)
TEST FOR THE DETERMINATION OF PEPTIDE C.
Registration Information
Analysis ID
635R2019 SSA
Registration Date
March 27, 2019
Manufacturer / Fabricante
Name (English)
ABBOTT LABORATORIES DE MEXICO SA DE CV