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ARA-TEM ® - INVIMA Registration b04535c2409e3be16b3178774d450d2d

Access comprehensive regulatory information for ARA-TEM ® (NOW-TEM ®) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID b04535c2409e3be16b3178774d450d2d and manufactured by WERFEN COLOMBIA SAS. The device was registered on December 20, 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
b04535c2409e3be16b3178774d450d2d
ARA-TEM ®
INVIMA Analysis ID: b04535c2409e3be16b3178774d450d2d
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Device Classification
Risk Class / Clase de Riesgo
II
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
b04535c2409e3be16b3178774d450d2d
Expire Date
December 20, 2027
Authorized Company / Fabricante
Name (Spanish)
WERFEN COLOMBIA SAS
Name (English)
THROW COLOMBIA SAS