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CAPTURE-P® READY-SCREEN - INVIMA Registration b977a968c4ceef8a3248dd42869f4f4a

Access comprehensive regulatory information for CAPTURE-P® READY-SCREEN (CAPTURE-P® READY-SCREEN) in the Colombia medical device market through Pure Global AI's free database. This III medical device is registered under INVIMA analysis ID b977a968c4ceef8a3248dd42869f4f4a and manufactured by IMMUCOR INC.. The device was registered on June 02, 2027.

This page provides complete registration details including product type (DIAGNOSTIC REAGENT), authorised information, and regulatory compliance data from the official Colombia INVIMA medical device database. Pure Global AI offers free access to Colombia's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate INVIMA regulations efficiently.

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INVIMA Official Data
III
b977a968c4ceef8a3248dd42869f4f4a
CAPTURE-P® READY-SCREEN
INVIMA Analysis ID: b977a968c4ceef8a3248dd42869f4f4a
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Product Use / Uso del Producto
Spanish

CAPTURE-P® READY-SCREEN® SOLID PHASE SYSTEM SE_x000D_ UTILIZA PARA DETECTAR IGG HLA Y ANTICUERPOS _x000D_ ESPECÍFICOS DE PLAQUETAS FRENTE A PLAQUETAS

English

CAPTURE-P® READY-SCREEN® SOLID PHASE SYSTEM SE_x000D_ USED TO DETECT HLA IGG AND ANTIBODIES _x000D_ PLATELET-SPECIFIC VS. PLATELET-SPECIFIC

Device Classification
Risk Class / Clase de Riesgo
III
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
b977a968c4ceef8a3248dd42869f4f4a
Expire Date
June 02, 2027
Authorized Company / Fabricante
Name (Spanish)
IMMUCOR INC.
Name (English)
IMMUCOR INC.