Pure Global

ATELLICA CH LACTATE DEHYDROGENASE L-P (LDLP) - INVIMA Registration 8a745598286418d990bbc26918c2ba94

Access comprehensive regulatory information for ATELLICA CH LACTATE DEHYDROGENASE L-P (LDLP) (ATELLICA CH LACTATE DEHYDROGENASE L-P (LDLP)) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 8a745598286418d990bbc26918c2ba94 and manufactured by SIEMENS HEALTHCARE S.A.S.. The device was registered on March 09, 2028.

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.

Free Database
Powered by Pure Global AI
INVIMA Official Data
II
8a745598286418d990bbc26918c2ba94
ATELLICA CH LACTATE DEHYDROGENASE L-P (LDLP)
INVIMA Analysis ID: 8a745598286418d990bbc26918c2ba94
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
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
8a745598286418d990bbc26918c2ba94
Expire Date
March 09, 2028
Authorized Company / Fabricante
Name (English)
SIEMENS HEALTHCARE S.A.S.