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Colombia INVIMA registration INVIMA 2025RD-0009150

1 AD-BIO® CASSETTE DE PRUEBA RÁPIDA COMBINADADE ROTAVIRUS Y ADENOVIRUS (HECES)

HEALGEN SCIENTIFIC LIMITED LIABILITY COMPANYIIColombia INVIMAExpires April 01, 2035
VerifiedINVIMA · official registry
Device classification
Registered product (Spanish)
1 AD-BIO® CASSETTE DE PRUEBA RÁPIDA COMBINADADE ROTAVIRUS Y ADENOVIRUS (HECES)
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Risk class / Clase de riesgo
II
Product group (Spanish)
REACTIVO DIAGNOSTICO
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Registration information
Sanitary registration
INVIMA 2025RD-0009150
Expediente
20302695
Status / Estado
Active
Expiry date
April 01, 2035
Registration holder / Titular
Name
ANNAR DIAGNOSTICA IMPORT S.A.S.
Associated party / Rol
Name
HEALGEN SCIENTIFIC LIMITED LIABILITY COMPANY
Role
FABRICANTE
Country
ESTADOS UNIDOS DE AMÉRICA
Manufacturer
HEALGEN SCIENTIFIC LIMITED LIABILITY COMPANY
About this record

Access comprehensive regulatory information for 1 AD-BIO® CASSETTE DE PRUEBA RÁPIDA COMBINADADE ROTAVIRUS Y ADENOVIRUS (HECES) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA sanitary registration INVIMA 2025RD-0009150, held by ANNAR DIAGNOSTICA IMPORT S.A.S. and associated with HEALGEN SCIENTIFIC LIMITED LIABILITY COMPANY (FABRICANTE). The registration expires on April 01, 2035.

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.