AD-BIO® PRUEBA RÁPIDA EN CASSETTE PARA DETECCIÓN DE ANTÍGENOS DE INFLUENZA A Y B (HISOPO)
- Registered product (Spanish)
- AD-BIO® PRUEBA RÁPIDA EN CASSETTE PARA DETECCIÓN DE ANTÍGENOS DE INFLUENZA A Y B (HISOPO)
- Risk class / Clase de riesgo
- III
- Sanitary registration
- INVIMA 2025RD-0009132
- Expediente
- 20298387
- Status / Estado
- Active
- Expiry date
- March 19, 2030
- Role
- FABRICANTE
- Country
- ESTADOS UNIDOS DE AMÉRICA
- Manufacturer
- HEALGEN SCIENTIFIC LIMITED LIABILITY COMPANY
Access comprehensive regulatory information for AD-BIO® PRUEBA RÁPIDA EN CASSETTE PARA DETECCIÓN DE ANTÍGENOS DE INFLUENZA A Y B (HISOPO) in the Colombia medical device market through Pure Global AI's free database. This III medical device is registered under INVIMA sanitary registration INVIMA 2025RD-0009132, held by ANNAR DIAGNOSTICA IMPORT S.A.S. and associated with HEALGEN SCIENTIFIC LIMITED LIABILITY COMPANY (FABRICANTE). The registration expires on March 19, 2030.
This page provides complete registration details including product group (REACTIVO DIAGNOSTICO), holder and associated-party information, and regulatory 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.