LDH 21 FS - INVIMA Registration 55280ebdc37141b19b28e2bd14dc5762
Access comprehensive regulatory information for LDH 21 FS (LDH 21 FS) in the Colombia medical device market through Pure Global AI's free database. This medical device is registered under INVIMA analysis ID 55280ebdc37141b19b28e2bd14dc5762 and manufactured by ANALISIS TECNICOS LTDA. The device was registered on November 17, 2031.
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
55280ebdc37141b19b28e2bd14dc5762
LDH 21 FS
INVIMA Analysis ID: 55280ebdc37141b19b28e2bd14dc5762
Device Classification
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
55280ebdc37141b19b28e2bd14dc5762
Expire Date
November 17, 2031
Authorized Company / Fabricante
Name (Spanish)
ANALISIS TECNICOS LTDAName (English)
ANALISIS TECNICOS LTDA

