5. SOPHIA DDM™ HOMOLOGOUS RECOMBINATION DEFICIENCY SOLUTION (HRD_V1) V1 - INVIMA Registration 94820ed9e9be51f5ecd00d48c32282fb
Access comprehensive regulatory information for 5. SOPHIA DDM™ HOMOLOGOUS RECOMBINATION DEFICIENCY SOLUTION (HRD_V1) V1 (5. SOPHIA DDM™ HOMOLOGOUS RECOMBINATION DEFICIENCY SOLUTION (HRD_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 94820ed9e9be51f5ecd00d48c32282fb 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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