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21.BIOSPIN PLASMA CIRCULATING DNA MIDI PURIFICATION KIT - INVIMA Registration 29d47455665597aec310756edd3fd601

Access comprehensive regulatory information for 21.BIOSPIN PLASMA CIRCULATING DNA MIDI PURIFICATION KIT (21.BIOSPIN PLASMA CIRCULATING DNA MIDI PURIFICATION KIT) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID 29d47455665597aec310756edd3fd601 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
29d47455665597aec310756edd3fd601
21.BIOSPIN PLASMA CIRCULATING DNA MIDI PURIFICATION KIT
INVIMA Analysis ID: 29d47455665597aec310756edd3fd601
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Product Use / Uso del Producto
Spanish

PRODUCTOS COMPLEMENTARIOS PARA BIOLOGรA_x000D_ MOLECULAR

English

COMPLEMENTARY PRODUCTS FOR BIOLOGรA_x000D_ MOLECULAR

Device Classification
Risk Class / Clase de Riesgo
I
Product Type (Spanish)
REACTIVOS IN VITRO
Product Type (English)
REACTIVOS IN VITRO
Registration Information
Analysis ID
29d47455665597aec310756edd3fd601
Expire Date
March 14, 2033
Authorized Company / Fabricante
Name (Spanish)
GENTECH S.A.S
Name (English)
GENTECH S.A.S