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4. SOPHIA DDM™ SOLID TUMOR PLUS SOLUTION (STS PLUS_V1) V1 - INVIMA Registration d80e48847219d2d64effb612d54f0719

Access comprehensive regulatory information for 4. SOPHIA DDM™ SOLID TUMOR PLUS SOLUTION (STS PLUS_V1) V1 (4. SOPHIA DDM™ SOLID TUMOR PLUS SOLUTION (STS PLUS_V1) V1 ) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID d80e48847219d2d64effb612d54f0719 and manufactured by SOPHIA GENETICS S.A. The device was registered on May 03, 2033.

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
I
d80e48847219d2d64effb612d54f0719
4. SOPHIA DDM™ SOLID TUMOR PLUS SOLUTION (STS PLUS_V1) V1
INVIMA Analysis ID: d80e48847219d2d64effb612d54f0719
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Product Use / Uso del Producto
Spanish

KITS PARA EL ANÁLISIS DE DATOS GENÓMICOS PRODUCIDOS POR SECUENCIADORES DE PRÓXIMA GENERACIÓN (NGS)._x000D_ TODOS LOS TIPOS DE VARIANTES GENÓMICAS. RESEARCH USE ONLY (PARA USO EXCLUSIVO EN INVESTIGACIÓN)

English

KITS FOR THE ANALYSIS OF GENOMIC DATA PRODUCED BY NEXT-GENERATION SEQUENCERS (NGS)._x000D_ ALL TYPES OF GENOMIC VARIANTS. RESEARCH USE ONLY (PARA USO EXCLUSIVO EN INVESTIGACIÓN)

Device Classification
Risk Class / Clase de Riesgo
I
Product Type (Spanish)
REACTIVOS IN VITRO
Product Type (English)
REACTIVOS IN VITRO
Registration Information
Analysis ID
d80e48847219d2d64effb612d54f0719
Expire Date
May 03, 2033
Authorized Company / Fabricante
Name (Spanish)
SOPHIA GENETICS S.A
Name (English)
SOPHIA GENETICS S.A