Pure Global

TUBO DE SUCCION - BIOLIFE Y GOLDENCARE - INVIMA Registration 50af18aca6a93d4e8ff2bc1534b3dfe1

Access comprehensive regulatory information for TUBO DE SUCCION - BIOLIFE Y GOLDENCARE (SUCTION TUBE - BIOLIFE AND GOLDENCARE) in the Colombia medical device market through Pure Global AI's free database. This IIa medical device is registered under INVIMA analysis ID 50af18aca6a93d4e8ff2bc1534b3dfe1 and manufactured by BIOPLAST S.A.S. The device was registered on March 19, 2031.

This page provides complete registration details including product type (SURGICAL DOCTOR), 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
IIa
50af18aca6a93d4e8ff2bc1534b3dfe1
TUBO DE SUCCION - BIOLIFE Y GOLDENCARE
INVIMA Analysis ID: 50af18aca6a93d4e8ff2bc1534b3dfe1
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Product Use / Uso del Producto
Spanish

ASPIRACION Y SUCCION DE SECRECIONES Y/O FLUIDOS

English

ASPIRATION AND SUCTION OF SECRETIONS AND/OR FLUIDS

Device Classification
Risk Class / Clase de Riesgo
IIa
Product Type (Spanish)
MEDICO QUIRURGICOS
Product Type (English)
SURGICAL DOCTOR
Registration Information
Analysis ID
50af18aca6a93d4e8ff2bc1534b3dfe1
Expire Date
March 19, 2031
Authorized Company / Fabricante
Name (Spanish)
BIOPLAST S.A.S
Name (English)
BIOPLAST S.A.S