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ORTHO ANTI-K (ANTI-KEL2) - INVIMA Registration d3f5dbc7d6509d33ec2d8dcff31924cd

Access comprehensive regulatory information for ORTHO ANTI-K (ANTI-KEL2) (Ortho anti-K (anti-Kel2)) in the Colombia medical device market through Pure Global AI's free database. This III medical device is registered under INVIMA analysis ID d3f5dbc7d6509d33ec2d8dcff31924cd and manufactured by ORTHO - CLINICAL DIAGNOSTICS COLOMBIA S.A.S. The device was registered on August 27, 2029.

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
III
d3f5dbc7d6509d33ec2d8dcff31924cd
ORTHO ANTI-K (ANTI-KEL2)
INVIMA Analysis ID: d3f5dbc7d6509d33ec2d8dcff31924cd
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Product Use / Uso del Producto
Spanish

PARA USO EN DIAGNร“STICO IN VITRO. PRUEBA _x000D_ CUALITATIVA PARA EL RECONOCIMIENTO DEL K-ANTรGENO _x000D_ (KEL2) EN LOS HEMATรES HUMANOS.

English

FOR USE IN VITRO DIAGNOSTICS. TRY _x000D_ QUALITATIVE FOR K-ANTIGEN RECOGNITION _x000D_ (KEL2) IN HUMAN RED BLOOD CELLS.

Device Classification
Risk Class / Clase de Riesgo
III
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
d3f5dbc7d6509d33ec2d8dcff31924cd
Expire Date
August 27, 2029
Authorized Company / Fabricante
Name (English)
ORTHO - CLINICAL DIAGNOSTICS COLOMBIA S.A.S