28aa107fc7c96fb41daecdd3eecce62f

DIACLON RH SUBGRUPOS + CW+K

BIOCIENTIFICA LTDA.·III·Colombia INVIMA·Expires May 23, 2029

Device classification

Risk class / Clase de Riesgo: III
Product type (Spanish): REACTIVO DIAGNOSTICO
Product type (English): DIAGNOSTIC REAGENT

Registration information

Analysis ID: 28aa107fc7c96fb41daecdd3eecce62f
Expire date: May 23, 2029

Authorized company / Fabricante

Name (Spanish): BIOCIENTIFICA LTDA.
Name (English): BIOSCIENTIFIC LTDA.

Product use / Uso del Producto

Spanish

ESTA TARJETA ID SIRVE PARA LA DETERMINACIÓN MANUAL_x000D_ Y EN INSTRUMENTOS DE LOS ANTÍGENOS C (RH2), C (RH8),_x000D_ C (RH4), E (RH3), E (RH5) Y K (KEL1) EN ERITROCITOS _x000D_ HUMANOS. PARA LA UTILIZACIÓN EN SISTEMAS _x000D_ SEMIAUTOMATIZADOS O TOTALMENTE AUTOMATIZADOS _x000D_ CONSULTE ELMANUAL DE USUARIO CORRESPONDIENTE.

English

THIS ID CARD IS USED TO DETERMINE MANUAL_x000D_ AND IN INSTRUMENTS OF THE ANTIGENS C (RH2), C (RH8),_x000D_ C (RH4), E (RH3), E (RH5) AND K (KEL1) IN ERYTHROCYTES _x000D_ HUMAN. FOR USE IN _x000D_ SYSTEMS SEMI-AUTOMATED OR FULLY AUTOMATED _x000D_ PLEASE REFER TO THE RELEVANT USER MANUAL.

About this record

Access comprehensive regulatory information for DIACLON RH SUBGRUPOS + CW+K (DIACLON RH SUBGRUPOS + CW+K) in the Colombia medical device market through Pure Global AI's free database. This III medical device is registered under INVIMA analysis ID 28aa107fc7c96fb41daecdd3eecce62f and manufactured by BIOCIENTIFICA LTDA.. The device was registered on May 23, 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.