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C2 CALIBRATION SOLUTION 2 - INVIMA Registration ee25082002d0942b420c66924d0e57f8

Access comprehensive regulatory information for C2 CALIBRATION SOLUTION 2 (C2 CALIBRATION SOLUTION 2) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID ee25082002d0942b420c66924d0e57f8 and manufactured by ROCHE DIAGNOSTICS GMBH (FABRICANTE PRODUCTO TERMINADO). The device was registered on October 02, 2027.

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
ee25082002d0942b420c66924d0e57f8
C2 CALIBRATION SOLUTION 2
INVIMA Analysis ID: ee25082002d0942b420c66924d0e57f8
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Product Use / Uso del Producto
Spanish

DETERMINACIร“N DE LOS DIFERENTES ANALITOS RELACIONADOS CON MUESTRAS PROCEDENTES DEL ORGANISMO HUMANO

English

DETERMINATION OF THE DIFFERENT ANALYTES RELATED TO SAMPLES FROM THE HUMAN ORGANISM

Device Classification
Risk Class / Clase de Riesgo
II
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
ee25082002d0942b420c66924d0e57f8
Expire Date
October 02, 2027
Authorized Company / Fabricante
Name (English)
ROCHE DIAGNOSTICS GMBH (FINISHED PRODUCT MANUFACTURER)