6921f1beacebf6ed6afa70a9f14e450f
IGF-I ELISA
BYO COLOMBIA S.A.S.·Colombia INVIMA·Expires August 11, 2031
Device classification
- Product type (Spanish)
- REACTIVO DIAGNOSTICO
- Product type (English)
- DIAGNOSTIC REAGENT
Registration information
- Analysis ID
- 6921f1beacebf6ed6afa70a9f14e450f
- Expire date
- August 11, 2031
Authorized company / Fabricante
- Name (Spanish)
- BYO COLOMBIA S.A.S.
- Name (English)
- BYO COLOMBIA S.A.S.
About this record
Access comprehensive regulatory information for IGF-I ELISA (IGF-I ELISA) in the Colombia medical device market through Pure Global AI's free database. This medical device is registered under INVIMA analysis ID 6921f1beacebf6ed6afa70a9f14e450f and manufactured by BYO COLOMBIA S.A.S.. The device was registered on August 11, 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.