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PID ORIENTATION TUBE - COFEPRIS Registration 1998R2021 SSA

Access comprehensive regulatory information for PID ORIENTATION TUBE (PID ORIENTATION TUBE) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1998R2021 SSA and manufactured by DICIPA, S.A. DE C.V.. The device was registered on November 29, 2021.

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
1998R2021 SSA
PID ORIENTATION TUBE
COFEPRIS Analysis ID: 1998R2021 SSA
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Product Use / Uso del Producto
Spanish

EL KIT PID ORIENTATION TUBE PUEDEUTILIZARSEPARAELESTUDIODEDEFECTOSNUMÉRICOS Y ALTERACIONES EN LADISTRIBUCIÓNRELATIVADELASDIFERENTESPOBLACIONES Y SUBPOBLACIONESLEUCOCITARIAS (CÉLULAS PRESENTADORASDEANTÍGENO,LINFOCITOSTYB NAIVE,DEMEMORIA Y EFECTORAS, ETC.).

English

THE PID ORIENTATION TUBE KIT CAN BE USED SEPARATELY TO STUDY NUMERICAL DEFECTS AND ALTERATIONS IN THE RELATIVE DISTRIBUTION OF DIFFERENT LEUKOCYTE POPULATIONS AND SUBPOPULATIONS (ANTIGEN-PRESENTING CELLS, NAÏVE TYB LYMPHOCYTES, MEMORY AND EFFECTORS, ETC.).

Device Classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
III. AGENTES DE DIAGNÓSTICO
Product Type (English)
III. DIAGNOSTIC AGENTS
Trade Name (Spanish)
KIT DE DIAGNÓSTICO IN VITRO PARAINMUNODEFICIENCIASPORCITOMETRÍADEFLUJO.
Trade Name (English)
IN VITRO DIAGNOSTIC KIT FORIMMUNODEFICIENCIESSPORCYTOMETRYFLOW FLOW.
Registration Information
Analysis ID
1998R2021 SSA
Registration Date
November 29, 2021
Manufacturer / Fabricante
Name (Spanish)
DICIPA, S.A. DE C.V.
Name (English)
DICIPA, S.A. DE C.V.