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NOVA LITE® MONKEY OESOPHAGUS IFA (CONJUGADO IGG-IGA) - INVIMA Registration b7a12195305230f7e7d761c71406c1f8

Access comprehensive regulatory information for NOVA LITE® MONKEY OESOPHAGUS IFA (CONJUGADO IGG-IGA) (NOVA LITE® MONKEY OESOPHAGUS IFA (CONJUGADO IGG-IGA) ) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID b7a12195305230f7e7d761c71406c1f8 and manufactured by WERFEN COLOMBIA S.A.S. The device was registered on August 10, 2032.

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
b7a12195305230f7e7d761c71406c1f8
NOVA LITE® MONKEY OESOPHAGUS IFA (CONJUGADO IGG-IGA)
INVIMA Analysis ID: b7a12195305230f7e7d761c71406c1f8
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Product Use / Uso del Producto
Spanish

SCREENING DE ANTICUERPOS CONTRA ANTIGENOS INTRAEPIDERMALES O ZONAS DE MMBRANA BASAL EN EL SUERO HUMANO PARA EL APOYO EN EL DIAGNOSTICO DE PENFIGO Y PENFIGOIDE BULLOSO

English

SCREENING OF ANTIBODIES AGAINST INTRAEPIDERMAL ANTIGENS OR BASAL MMBRANA ZONES IN HUMAN SERUM FOR SUPPORT IN THE DIAGNOSIS OF PEMPHIGUS AND BULLOUS PEMPHIGOID

Device Classification
Risk Class / Clase de Riesgo
II
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
b7a12195305230f7e7d761c71406c1f8
Expire Date
August 10, 2032
Authorized Company / Fabricante
Name (Spanish)
WERFEN COLOMBIA S.A.S
Name (English)
THROW COLOMBIA S.A.S