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2.BIOSPIN PLASMID DNA MIDI EXTRACTION KIT - INVIMA Registration 42132c50c7336442af6991cf4e99adf5

Access comprehensive regulatory information for 2.BIOSPIN PLASMID DNA MIDI EXTRACTION KIT (2.BIOSPIN PLASMID DNA MIDI EXTRACTION KIT) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID 42132c50c7336442af6991cf4e99adf5 and manufactured by GENTECH S.A.S. The device was registered on March 14, 2033.

This page provides complete registration details including product type (REACTIVOS IN VITRO), 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
I
42132c50c7336442af6991cf4e99adf5
2.BIOSPIN PLASMID DNA MIDI EXTRACTION KIT
INVIMA Analysis ID: 42132c50c7336442af6991cf4e99adf5
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Product Use / Uso del Producto
Spanish

PRODUCTOS COMPLEMENTARIOS PARA BIOLOGรA_x000D_ MOLECULA

English

COMPLEMENTARY PRODUCTS FOR BIOLOGรA_x000D_ MOLECULE

Device Classification
Risk Class / Clase de Riesgo
I
Product Type (Spanish)
REACTIVOS IN VITRO
Product Type (English)
REACTIVOS IN VITRO
Registration Information
Analysis ID
42132c50c7336442af6991cf4e99adf5
Expire Date
March 14, 2033
Authorized Company / Fabricante
Name (Spanish)
GENTECH S.A.S
Name (English)
GENTECH S.A.S