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16. BIOEASY MULTIPLEX QPCR PROBE MASTER MIX I (UDG PLUS) - INVIMA Registration 429c9702edd9024fe433db3637e7e3f6

Access comprehensive regulatory information for 16. BIOEASY MULTIPLEX QPCR PROBE MASTER MIX I (UDG PLUS) (16. BIOEASY MULTIPLEX QPCR PROBE MASTER MIX I (UDG PLUS)) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID 429c9702edd9024fe433db3637e7e3f6 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
429c9702edd9024fe433db3637e7e3f6
16. BIOEASY MULTIPLEX QPCR PROBE MASTER MIX I (UDG PLUS)
INVIMA Analysis ID: 429c9702edd9024fe433db3637e7e3f6
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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
429c9702edd9024fe433db3637e7e3f6
Expire Date
March 14, 2033
Authorized Company / Fabricante
Name (Spanish)
GENTECH S.A.S
Name (English)
GENTECH S.A.S