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ELECSYS AMH PLUS (HORMONA ANTI-MULLERIANA) - INVIMA Registration a3cffad70f1bc3483ac81e077798e3e2

Access comprehensive regulatory information for ELECSYS AMH PLUS (HORMONA ANTI-MULLERIANA) (ELECSYS AMH PLUS (HORMONA ANTI-MULLERIANA)) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID a3cffad70f1bc3483ac81e077798e3e2 and manufactured by ROCHE DIAGNOSTICS GMBH. The device was registered on May 08, 2034.

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
a3cffad70f1bc3483ac81e077798e3e2
ELECSYS AMH PLUS (HORMONA ANTI-MULLERIANA)
INVIMA Analysis ID: a3cffad70f1bc3483ac81e077798e3e2
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Product Use / Uso del Producto
Spanish

DETERMINACIร“N DE LOS DIFERENTES ANALITOS RELACIONADOS CON MUESTRAS PROCEDENTES DEL ORGANISMO HUMANO

English

DETERMINATION OF THE DIFFERENT ANALYTES RELATED TO SAMPLES FROM THE HUMAN ORGANISM

Device Classification
Risk Class / Clase de Riesgo
II
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
a3cffad70f1bc3483ac81e077798e3e2
Expire Date
May 08, 2034
Authorized Company / Fabricante
Name (English)
ROCHE DIAGNOSTICS GMBH