COPRO SYSTEM Plus - ARCSA Registration 9151b0c0b68efa9afc3ba225ee4015a7
Access comprehensive regulatory information for COPRO SYSTEM Plus in the Ecuador medical device market through Pure Global AI's free database. This I medical device is registered under ARCSA ID 9151b0c0b68efa9afc3ba225ee4015a7 and manufactured by LIOFILCHEM S.R.L. The device was registered on February 13, 2023.
This page provides complete registration details including product type (In Vitro Diagnostic), manufacturer information, authorized representative details, and regulatory compliance data from the official Ecuador ARCSA medical device database. Pure Global AI offers free access to Ecuador's complete medical device registry.
Free Database
Powered by Pure Global AI
ARCSA Official Data
I
9151b0c0b68efa9afc3ba225ee4015a7
COPRO SYSTEM Plus
ARCSA ID: 9151b0c0b68efa9afc3ba225ee4015a7
Device Classification
Risk Class
I
Product Type
In Vitro Diagnostic
Brand Name
LIOFILCHEM
Commercial Name
19-200 IVD Reagents/Testing Kits, Microbiology, Bacteria
Registration Information
Analysis ID
9151b0c0b68efa9afc3ba225ee4015a7
Registration Date
February 13, 2023
Expiration Date
February 13, 2028
Product Use
SYSTEM FOR THE DETECTION AND PRESUMPTIVE IDENTIFICATION OF INTESTINAL PATHOGENIC MICROORGANISMS
Manufacturer
Name
LIOFILCHEM S.R.LCity
TERAMO - ITALY
Country
ITALY
Address
CALLE ZONA INDUSTRIALE, 64026 ROSETO DEGLI ARUZZI, ITALY
Product Owner
Name
LIOFILCHEM S.R.L
Country
ITALY
Authorized Representative