Pure Global

SERAZYM ADENOVIRUS - INVIMA Registration b095bef0ce6d326be21ce1b8161a618e

Access comprehensive regulatory information for SERAZYM ADENOVIRUS (SERAZYM ADENOVIRUS) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID b095bef0ce6d326be21ce1b8161a618e and manufactured by BYO COLOMBIA S.A.S.. The device was registered on March 14, 2033.

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
b095bef0ce6d326be21ce1b8161a618e
SERAZYM ADENOVIRUS
INVIMA Analysis ID: b095bef0ce6d326be21ce1b8161a618e
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 _x000D_ RELACIONADOS CON MUESTRAS PROCEDENTES DEL _x000D_ ORGANISMO HUMANO

English

DETERMINATION OF THE DIFFERENT ANALYTES _x000D_ RELATED TO SAMPLES FROM THE _x000D_ HUMAN ORGANISM

Device Classification
Risk Class / Clase de Riesgo
II
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
b095bef0ce6d326be21ce1b8161a618e
Expire Date
March 14, 2033
Authorized Company / Fabricante
Name (Spanish)
BYO COLOMBIA S.A.S.
Name (English)
BYO COLOMBIA S.A.S.