Pure Global

NEXTSEQ™ 1000/2000 P2 REAGENTS - INVIMA Registration 3e2d457a8bd3d8b6af7028b4d62dc9a9

Access comprehensive regulatory information for NEXTSEQ™ 1000/2000 P2 REAGENTS (NEXTSEQ™ 1000/2000 P2 REAGENTS) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID 3e2d457a8bd3d8b6af7028b4d62dc9a9 and manufactured by ILLUMINA COLOMBIA S.A.S.. The device was registered on February 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.

Free Database
Powered by Pure Global AI
INVIMA Official Data
I
3e2d457a8bd3d8b6af7028b4d62dc9a9
NEXTSEQ™ 1000/2000 P2 REAGENTS
INVIMA Analysis ID: 3e2d457a8bd3d8b6af7028b4d62dc9a9
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Device Classification
Risk Class / Clase de Riesgo
I
Product Type (Spanish)
REACTIVOS IN VITRO
Product Type (English)
REACTIVOS IN VITRO
Registration Information
Analysis ID
3e2d457a8bd3d8b6af7028b4d62dc9a9
Expire Date
February 14, 2033
Authorized Company / Fabricante
Name (English)
ILLUMINA COLOMBIA S.A.S.