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MULTI SAMPLE NEEDLE (AGUJA MULTIMUESTRA) - COFEPRIS Registration 642E2019 SSA

Access comprehensive regulatory information for MULTI SAMPLE NEEDLE (AGUJA MULTIMUESTRA) (MULTI SAMPLE NEEDLE (AGUJA MULTIMUESTRA)) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 642E2019 SSA and manufactured by ATYDE MÉXICO, S.A. DE C.V.. The device was registered on March 28, 2019.

This page provides complete registration details including product type (I. MEDICAL EQUIPMENT), 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
642E2019 SSA
MULTI SAMPLE NEEDLE (AGUJA MULTIMUESTRA)
COFEPRIS Analysis ID: 642E2019 SSA
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Product Use / Uso del Producto
Spanish

LA AGUJA MULTIMUESTRA PARA RECOLECCIÓN DE SANGRE SE UTILIZA JUNTO CON EL TUBO DE RECOLECCIÓN DE SANGRE AL VACÍO Y EL SOSTENEDOR DE LA AGUJA. ÉSTOS COMPONEN EL SISTEMA DE RECOLECCIÓN DE SANGRE AL VACÍO, PARA SER UTILIZADO EN LA COLECCIÓN DE SANGRE VENOSA.

English

THE MULTI-SAMPLE BLOOD COLLECTION NEEDLE IS USED IN CONJUNCTION WITH THE VACUUM BLOOD COLLECTION TUBE AND NEEDLE HOLDER. THESE MAKE UP THE VACUUM BLOOD COLLECTION SYSTEM, TO BE USED IN VENOUS BLOOD COLLECTION.

Device Classification
Risk Class / Clase de Riesgo
Clase II
Product Type (Spanish)
I. EQUIPO MÉDICO
Product Type (English)
I. MEDICAL EQUIPMENT
Trade Name (Spanish)
AGUJA MULTIMUESTRA
Trade Name (English)
MULTISAMPLE AGUJA
Registration Information
Analysis ID
642E2019 SSA
Registration Date
March 28, 2019
Manufacturer / Fabricante
Name (English)
ATYDE MÉXICO, S.A. DE C.V.