QUANTA Lite Histone 708520 - ARCSA Registration ad595d05987da307f3aa20d9a4bc81a2
Access comprehensive regulatory information for QUANTA Lite Histone 708520 in the Ecuador medical device market through Pure Global AI's free database. This III medical device is registered under ARCSA ID ad595d05987da307f3aa20d9a4bc81a2 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
ad595d05987da307f3aa20d9a4bc81a2
QUANTA Lite Histone
708520
ARCSA ID: ad595d05987da307f3aa20d9a4bc81a2
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
ad595d05987da307f3aa20d9a4bc81a2
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