AD-BIO® PRUEBA RÁPIDA DE IGG/IGM DEL VIRUS DE LA HEPATITIS A VHA (SANGRE TOTAL/ SUERO/ PLASMA) (CASSETTE)
- Registered product (Spanish)
- AD-BIO® PRUEBA RÁPIDA DE IGG/IGM DEL VIRUS DE LA HEPATITIS A VHA (SANGRE TOTAL/ SUERO/ PLASMA) (CASSETTE)
- Risk class / Clase de riesgo
- III
- Sanitary registration
- INVIMA 2025RD-0009187
- Expediente
- 20302556
- Status / Estado
- Active
- Expiry date
- May 08, 2030
- Role
- FABRICANTE
- Country
- ESTADOS UNIDOS DE AMÉRICA
- Manufacturer
- HEALGEN SCIENTIFIC LIMITED LIABILITY COMPANY
Access comprehensive regulatory information for AD-BIO® PRUEBA RÁPIDA DE IGG/IGM DEL VIRUS DE LA HEPATITIS A VHA (SANGRE TOTAL/ SUERO/ PLASMA) (CASSETTE) 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-0009187, held by ANNAR DIAGNOSTICA IMPORT S.A.S. and associated with HEALGEN SCIENTIFIC LIMITED LIABILITY COMPANY (FABRICANTE). The registration expires on May 08, 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.