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QUANTA-Lite RNP 708565 - ARCSA Registration c1db7de0715c0edb33d537a2aced0cdb

Access comprehensive regulatory information for QUANTA-Lite RNP 708565 in the Ecuador medical device market through Pure Global AI's free database. This III medical device is registered under ARCSA ID c1db7de0715c0edb33d537a2aced0cdb and manufactured by INOVA DIAGNOSTIC INC. The device was registered on October 02, 2020.

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.

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ARCSA Official Data
III
c1db7de0715c0edb33d537a2aced0cdb
QUANTA-Lite RNP 708565
ARCSA ID: c1db7de0715c0edb33d537a2aced0cdb
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Device Classification
Risk Class
III
Product Type
In Vitro Diagnostic
Brand Name
INOVA
Commercial Name
19-173 Reagents DVI Test Kit, Immunoassay, Autoimmune
Registration Information
Analysis ID
c1db7de0715c0edb33d537a2aced0cdb
Registration Date
October 02, 2020
Expiration Date
October 02, 2025
Product Use

IN VITRO DIAGNOSTICS

Manufacturer
City
SAN DIEGO
Country
UNITED STATES
Address
9900 OLD GROVE RD, SAN DIEGO, CA 92131
Product Owner
Name
INOVA DIAGNOSTIC INC
Country
UNITED STATES
Authorized Representative
Address
VOZANDES N42-54 AND MARIANO ECHEVERRIA
Phone
26009479