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INNO-LIPA HLA- A - INVIMA Registration 8af633d2bbb68c68174d87ab193cd0d8

Access comprehensive regulatory information for INNO-LIPA HLA- A (INNO-LIPA HLA- A) in the Colombia medical device market through Pure Global AI's free database. This III medical device is registered under INVIMA analysis ID 8af633d2bbb68c68174d87ab193cd0d8 and manufactured by QUIMIOLAB S.A.S. The device was registered on October 04, 2029.

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
III
8af633d2bbb68c68174d87ab193cd0d8
INNO-LIPA HLA- A
INVIMA Analysis ID: 8af633d2bbb68c68174d87ab193cd0d8
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Product Use / Uso del Producto
Spanish

INNO-LIPA HLA- A MรšLTIPLEX, DE USO IN VITRO, ESTร DISEร‘ADO PARA LA AMPLIFICACIร“N DE LOS รCIDOS NUCLEICOS DEL PRIMERO AL CUARTO EXร“N DEL LOCUS A DEL ANTIGENO LEUCOCITARIO HUMANO (HLA). LA REACCIร“N SE LLEVA A CABO MEDIANTE LA REACCIร“N EN CADENA DE LA POLIMERASA (PCR) EN UN FORMATO MรšLTIPLE.

English

INNO-LIPA HLA- A MULTIPLEX, FOR IN VITRO USE, IS DESIGNED FOR ACID AMPLIFICATION NUCLEIC NUCLEIC FROM THE FIRST TO THE FOURTH EXON OF LOCUS A OF THE HUMAN LEUKOCYTE ANTIGEN (HLA). THE REACTION IT IS CARRIED OUT BY THE CHAIN REACTION OF POLYMERASE (PCR) IN A MULTIPLE FORMAT.

Device Classification
Risk Class / Clase de Riesgo
III
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
8af633d2bbb68c68174d87ab193cd0d8
Expire Date
October 04, 2029
Authorized Company / Fabricante
Name (Spanish)
QUIMIOLAB S.A.S
Name (English)
QUIMIOLAB S.A.S