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CD38-SNV605 - INVIMA Registration 5abe4e84bded205e13a34090b704c741

Access comprehensive regulatory information for CD38-SNV605 (CD38-SNV605) in the Colombia medical device market through Pure Global AI's free database. This medical device is registered under INVIMA analysis ID 5abe4e84bded205e13a34090b704c741 and manufactured by BECKMAN COULTER COLOMBIA SAS. The device was registered on April 12, 2032.

This page provides complete registration details including product type (REACTIVOS IN VITRO), 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
5abe4e84bded205e13a34090b704c741
CD38-SNV605
INVIMA Analysis ID: 5abe4e84bded205e13a34090b704c741
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Product Use / Uso del Producto
Spanish

REACTIVOS UTILIZADOS รšNICAMENTE EN INVESTIGACIร“N, NO DEBEN SER UTILIZADOS EN PROCEDIMIENTOS DE DIAGNร“STICO.

English

REAGENTS USED ONLY IN RESEARCH, SHOULD NOT BE USED IN DIAGNOSTIC PROCEDURES.

Device Classification
Product Type (Spanish)
REACTIVOS IN VITRO
Product Type (English)
REACTIVOS IN VITRO
Registration Information
Analysis ID
5abe4e84bded205e13a34090b704c741
Expire Date
April 12, 2032
Authorized Company / Fabricante
Name (English)
BECKMAN COULTER COLOMBIA SAS