EGFR (EP22) - INVIMA Registration fd0717e328c4395d6b2d6e892e539fa5

Access comprehensive regulatory information for EGFR (EP22) (EGFR (EP22)) in the Colombia medical device market through Pure Global AI's free database. This medical device is registered under INVIMA analysis ID fd0717e328c4395d6b2d6e892e539fa5 and manufactured by INMUNOTECH LABORATORIES S.A.S.. The device was registered on August 03, 2031.

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.