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COBAS INFLUENZA A/B & RSV QUALITY CONTROL KIT FOR USE ON THE COBAS LIAT SYSTEM - INVIMA Registration 5e2171db4572c4a9f8b61cd840c9f2cd

Access comprehensive regulatory information for COBAS INFLUENZA A/B & RSV QUALITY CONTROL KIT FOR USE ON THE COBAS LIAT SYSTEM (COBAS INFLUENZA A/B & RSV QUALITY CONTROL KIT FOR USE ON THE COBAS LIAT SYSTEM ) in the Colombia medical device market through Pure Global AI's free database. This III medical device is registered under INVIMA analysis ID 5e2171db4572c4a9f8b61cd840c9f2cd and manufactured by ROCHE DIAGNOSTICS GMBH (FABRICANTE PRODUCTO TERMINADO). The device was registered on April 26, 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
5e2171db4572c4a9f8b61cd840c9f2cd
COBAS INFLUENZA A/B & RSV QUALITY CONTROL KIT FOR USE ON THE COBAS LIAT SYSTEM
INVIMA Analysis ID: 5e2171db4572c4a9f8b61cd840c9f2cd
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Product Use / Uso del Producto
Spanish

KIT DE CONTROL DE CALIDAD PARA COBAS R INFLUENZA A/B & RSV PARA USO EN EL COBAS LIAT SYSTEM. ESTE KIT CONTIENE CONTROLES EXTERNOS PARA SU USO CON EL ENSAYO COBAS R INFLUENZA A/B & RSV. LOS CONTROLES EXTERNOS SE EJECUTAN DURANTE EL PROCEDIMIENTO PARA Aร‘ADIR LOTES DE TUBOS DE ENSAYO COBAS R INFLUENZA A/B & RSV. OTROS CONTROLES EXTERNOS DEBERIAN ANALIZARSE DE ACUERDO CON LOS REQUISITOS LOCALES, ESTATALES, FEDERALES Y/O DE ORGANIZACIONES DE ACREDITACION APLICABLES.

English

QUALITY CONTROL KIT FOR COBAS R INFLUENZA A/B & RSV FOR USE IN THE COBAS LIAT SYSTEM. THIS KIT CONTAINS EXTERNAL CONTROLS FOR USE WITH THE COBAS R INFLUENZA A/B & RSV ASSAY. EXTERNAL CONTROLS ARE PERFORMED DURING THE PROCEDURE FOR ADDING BATCHES OF COBAS R INFLUENZA A/B & RSV TEST TUBES. OTHER EXTERNAL CONTROLS SHOULD BE ANALYZED IN ACCORDANCE WITH APPLICABLE LOCAL, STATE, FEDERAL AND/OR ACCREDITATION ORGANIZATION REQUIREMENTS.

Device Classification
Risk Class / Clase de Riesgo
III
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
5e2171db4572c4a9f8b61cd840c9f2cd
Expire Date
April 26, 2029
Authorized Company / Fabricante
Name (English)
ROCHE DIAGNOSTICS GMBH (FINISHED PRODUCT MANUFACTURER)