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BIOLINE™ CHLAMYDIA - INVIMA Registration de6e48cedba61adb4fdcb33f1ee66804

Access comprehensive regulatory information for BIOLINE™ CHLAMYDIA ( BIOLINE™ CHLAMYDIA) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID de6e48cedba61adb4fdcb33f1ee66804 and manufactured by ABBOTT RAPID DIAGNOSTICS COLOMBIA S.A.S. The device was registered on March 22, 2033.

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.

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INVIMA Official Data
II
de6e48cedba61adb4fdcb33f1ee66804
BIOLINE™ CHLAMYDIA
INVIMA Analysis ID: de6e48cedba61adb4fdcb33f1ee66804
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Product Use / Uso del Producto
Spanish

DETECCION RAPIDA Y CUALITATIVA DEL ANTIGENO DE LA CHLAMYDIA DIRECTAMENTE UTILIZANDO HISOPADO ENDOCERVICAL Y HACIENDO UNA CITOLOGIA POR CEPILLADO.

English

RAPID AND QUALITATIVE DETECTION OF CHLAMYDIA ANTIGEN DIRECTLY USING ENDOCERVICAL SWAB AND BRUSHING CYTOLOGY.

Device Classification
Risk Class / Clase de Riesgo
II
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
de6e48cedba61adb4fdcb33f1ee66804
Expire Date
March 22, 2033
Authorized Company / Fabricante
Name (English)
ABBOTT RAPID DIAGNOSTICS COLOMBIA S.A.S