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ANTI-MYCOPLASMA PNEUMONIAE ELISA (IGG) - INVIMA Registration 69f69ff41f49ba5215761c2302226b0b

Access comprehensive regulatory information for ANTI-MYCOPLASMA PNEUMONIAE ELISA (IGG) (ANTI-MYCOPLASMA PNEUMONIAE ELISA (IGG)) in the Colombia medical device market through Pure Global AI's free database. This medical device is registered under INVIMA analysis ID 69f69ff41f49ba5215761c2302226b0b 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.

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INVIMA Official Data
69f69ff41f49ba5215761c2302226b0b
ANTI-MYCOPLASMA PNEUMONIAE ELISA (IGG)
INVIMA Analysis ID: 69f69ff41f49ba5215761c2302226b0b
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Device Classification
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
69f69ff41f49ba5215761c2302226b0b
Expire Date
December 15, 2030
Authorized Company / Fabricante
Name (Spanish)
BYO COLOMBIA SAS
Name (English)
BYO COLOMBIA SAS