Revogene® Instrument - ARCSA Registration 027d9f0a4241b28a8904b722428fea76
Access comprehensive regulatory information for Revogene® Instrument in the Ecuador medical device market through Pure Global AI's free database. This I medical device is registered under ARCSA ID 027d9f0a4241b28a8904b722428fea76 and manufactured by MERIDIAN BIOSCIENCE, INC.. The device was registered on April 07, 2022.
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
I
027d9f0a4241b28a8904b722428fea76
Revogene® Instrument
ARCSA ID: 027d9f0a4241b28a8904b722428fea76
Device Classification
Risk Class
I
Product Type
In Vitro Diagnostic
Brand Name
REVOGENE
Commercial Name
20-668 Analyzers, Laboratory, Molecular Assay
Sterilization Method
MOLECULAR DIAGNOSIS
Registration Information
Analysis ID
027d9f0a4241b28a8904b722428fea76
Registration Date
April 07, 2022
Expiration Date
April 07, 2027
Creation Date
July 04, 2022
Product Use
PERFORM NUCLEIC ACID TESTING OF SPECIFIC IVD ASSAYS IN CLINICAL LABORATORIES
Manufacturer
City
CINCINNATI
Country
UNITED STATES
Address
3471 RIVER HILLS DRIVE, CINCINNATI, OH 45244 USA
Product Owner
Name
MERIDIAN BIOSCIENCE, INC.
Country
UNITED STATES
Authorized Representative