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1. ORTHO BLISS - INVIMA Registration 40e5e6293d8cc6e7b5a5e705fc1bd97a

Access comprehensive regulatory information for 1. ORTHO BLISS (1. ORTHO BLISS) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 40e5e6293d8cc6e7b5a5e705fc1bd97a and manufactured by ORTHO - CLINICAL DIAGNOSTICS COLOMBIA S.A.S. The device was registered on December 17, 2030.

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
40e5e6293d8cc6e7b5a5e705fc1bd97a
1. ORTHO BLISS
INVIMA Analysis ID: 40e5e6293d8cc6e7b5a5e705fc1bd97a
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Product Use / Uso del Producto
Spanish

SOLUCIร’N DE CONCENTRACIร’N Iร’NICA BAJA (BLISS) PARA USAR CON EL SISTEMA ORTHO BIO VUE

English

LOW ION CONCENTRATION SOLUTION (BLISS) FOR USE WITH THE ORTHO BIO VUE SYSTEM

Device Classification
Risk Class / Clase de Riesgo
II
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
40e5e6293d8cc6e7b5a5e705fc1bd97a
Expire Date
December 17, 2030
Authorized Company / Fabricante
Name (English)
ORTHO - CLINICAL DIAGNOSTICS COLOMBIA S.A.S