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2. ANTI-TNFA-PE - INVIMA Registration bccf847288d6f37b2ac02a3caf917631

Access comprehensive regulatory information for 2. ANTI-TNFA-PE (2. ANTI-TNFA-PE) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID bccf847288d6f37b2ac02a3caf917631 and manufactured by BECKMAN COULTER COLOMBIA SAS. The device was registered on March 29, 2033.

This page provides complete registration details including product type (REACTIVOS IN VITRO), 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
I
bccf847288d6f37b2ac02a3caf917631
2. ANTI-TNFA-PE
INVIMA Analysis ID: bccf847288d6f37b2ac02a3caf917631
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Product Use / Uso del Producto
Spanish

INGREDIENTES ACTIVOS PARA Tร‰CNICAS IN-HOUSE (ASR)

English

ACTIVE INGREDIENTS FOR IN-HOUSE TECHNIQUES (ASR)

Device Classification
Risk Class / Clase de Riesgo
I
Product Type (Spanish)
REACTIVOS IN VITRO
Product Type (English)
REACTIVOS IN VITRO
Registration Information
Analysis ID
bccf847288d6f37b2ac02a3caf917631
Expire Date
March 29, 2033
Authorized Company / Fabricante
Name (English)
BECKMAN COULTER COLOMBIA SAS