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Revogene Carba C test kit - ARCSA Registration e5cc437b214dc7f0975cc8036949f806

Access comprehensive regulatory information for Revogene Carba C test kit in the Ecuador medical device market through Pure Global AI's free database. This II medical device is registered under ARCSA ID e5cc437b214dc7f0975cc8036949f806 and manufactured by MERIDIAN BIOSCIENCE, INC.. The device was registered on April 12, 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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II
e5cc437b214dc7f0975cc8036949f806
Revogene Carba C test kit
ARCSA ID: e5cc437b214dc7f0975cc8036949f806
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Device Classification
Risk Class
II
Product Type
In Vitro Diagnostic
Brand Name
REVOGENE
Commercial Name
19-238 IVD Reagents/Kits, Molecular Assay, Infection, Bacteria
Sterilization Method
MOLECULAR DIAGNOSIS
Registration Information
Analysis ID
e5cc437b214dc7f0975cc8036949f806
Registration Date
April 12, 2022
Expiration Date
April 12, 2027
Creation Date
December 04, 2022
Product Use

DETECTION AND DIFFERENTIATION OF GENE SEQUENCES BLAKPC, BLANDM, BLAVIM, BLATIPO OXA-48, AND BLAIMP RELATED TO PURE COLONIES OF ENTEROBACTERIACEAE, ACINETOBACTER BAUMANNII OR PSEUDOMONAS AERUGINOSA NOT SUSCEPTIBLE TO CARBAPENEMS

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
Address
GUAYAS 6-165
Phone
74091610