Xpert®Norovirus - ARCSA Registration cd7d6a855f434822eca766ba2cfa9c24
Access comprehensive regulatory information for Xpert®Norovirus in the Ecuador medical device market through Pure Global AI's free database. This III medical device is registered under ARCSA ID cd7d6a855f434822eca766ba2cfa9c24 and manufactured by CEPHEID AB. The device was registered on May 20, 2015.
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
cd7d6a855f434822eca766ba2cfa9c24
Xpert®Norovirus
ARCSA ID: cd7d6a855f434822eca766ba2cfa9c24
Device Classification
Risk Class
III
Product Type
In Vitro Diagnostic
Brand Name
XPERT®
Commercial Name
19-242 IVD Reagents/Kits, Molecular Assay, Infection, Viruses
Sterilization Method
Molecular diagnostics
Registration Information
Analysis ID
cd7d6a855f434822eca766ba2cfa9c24
Registration Date
May 20, 2015
Expiration Date
May 20, 2025
Creation Date
April 30, 2020
Product Use
QUALITATIVE TEST DESIGNED FOR THE IDENTIFICATION AND RAPID DIFFERENTIATION OF GENOGROUPS I AND II OF NOROVIRUS RNA
Manufacturer
Product Owner
Name
CEPHEID AB
Country
SWEDEN
Authorized Representative
Address
TODOS LOS SANTOS # 201 AND AV. JORGE PEREZ CONCHA
Phone
2610680