Pure Global

ANTI-MYCOPLASMA PNEUMONIAE ELISA (IGM) - INVIMA Registration 52c7ef3c8986daaef4a7aa896d789aee

Access comprehensive regulatory information for ANTI-MYCOPLASMA PNEUMONIAE ELISA (IGM) (ANTI-MYCOPLASMA PNEUMONIAE ELISA (IGM)) in the Colombia medical device market through Pure Global AI's free database. This medical device is registered under INVIMA analysis ID 52c7ef3c8986daaef4a7aa896d789aee and manufactured by BYO COLOMBIA SAS. The device was registered on December 15, 2030.

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
52c7ef3c8986daaef4a7aa896d789aee
ANTI-MYCOPLASMA PNEUMONIAE ELISA (IGM)
INVIMA Analysis ID: 52c7ef3c8986daaef4a7aa896d789aee
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Device Classification
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
52c7ef3c8986daaef4a7aa896d789aee
Expire Date
December 15, 2030
Authorized Company / Fabricante
Name (Spanish)
BYO COLOMBIA SAS
Name (English)
BYO COLOMBIA SAS