Pure Global

12. SOPHIA DDM CUSTOM SOLUTION (CCLL_A_V3) V3 - INVIMA Registration 4cfaf7571ae9cc94e14f32c1a9fc17aa

Access comprehensive regulatory information for 12. SOPHIA DDM CUSTOM SOLUTION (CCLL_A_V3) V3 (12. SOPHIA DDM CUSTOM SOLUTION (CCLL_A_V3) V3) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID 4cfaf7571ae9cc94e14f32c1a9fc17aa and manufactured by SOPHIA GENETICS S.A. The device was registered on December 07, 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.

Free Database
Powered by Pure Global AI
INVIMA Official Data
I
4cfaf7571ae9cc94e14f32c1a9fc17aa
12. SOPHIA DDM CUSTOM SOLUTION (CCLL_A_V3) V3
INVIMA Analysis ID: 4cfaf7571ae9cc94e14f32c1a9fc17aa
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Product Use / Uso del Producto
Spanish

KITS PARA EL ANรLISIS DE DATOS GENร“MICOS PRODUCIDOS POR SECUENCIADORES DE PRร“XIMA GENERACIร“N (NGS). TODOS_x000D_ LOS TIPOS DE VARIANTES GENร“MICAS. RESEARCH USE ONLY (PARA USO EXCLUSIVO EN INVESTIGACIร“N)

English

KITS FOR THE ANALYSIS OF GENOMIC DATA PRODUCED BY NEXT-GENERATION SEQUENCERS (NGS). TODOS_x000D_ THE TYPES OF GENOMIC VARIANTS. RESEARCH USE ONLY (PARA USO EXCLUSIVO EN INVESTIGACIร“N)

Device Classification
Risk Class / Clase de Riesgo
I
Product Type (Spanish)
REACTIVOS IN VITRO
Product Type (English)
REACTIVOS IN VITRO
Registration Information
Analysis ID
4cfaf7571ae9cc94e14f32c1a9fc17aa
Expire Date
December 07, 2033
Authorized Company / Fabricante
Name (Spanish)
SOPHIA GENETICS S.A
Name (English)
SOPHIA GENETICS S.A