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a76fdc98d34f6607316593a1470fecc7

Access Rubella IgG

BECKMAN COULTER, INC.·III·Ecuador ARCSA·Registered May 07, 2023
Device classification
Risk class
III
Product type
In Vitro Diagnostic
Brand name
BECKMAN COULTER
Commercial name
17-077 IVD Reagents/Testing Kits, Serology, Viruses
Registration information
Analysis ID
a76fdc98d34f6607316593a1470fecc7
Registration date
May 07, 2023
Expiration date
May 07, 2028
Manufacturer
Name
BECKMAN COULTER, INC.
City
BREA
Country
UNITED STATES
Address
250 S. KRAEMER BLVD BREA, CA USA 92821
Product owner
Name
BECKMAN COULTER, INC.
Country
UNITED STATES
Authorized representative
Name
FRISONEX FRISON IMPORTADORA EXPORTADORA CIA. LTDA.
Address
LAS AVELLANAS STREET E2-25 AND JUNCAL
Phone
23971600
Product use

QUALITATIVE AND QUANTITATIVE DETERMINATION OF IGG ANTIBODIES TO RUBELLA VIRUS IN HUMAN SERUM USING ACCESS IMMUNOASSAY SYSTEMS.

About this record

Access comprehensive regulatory information for Access Rubella IgG in the Ecuador medical device market through Pure Global AI's free database. This III medical device is registered under ARCSA ID a76fdc98d34f6607316593a1470fecc7 and manufactured by BECKMAN COULTER, INC.. The device was registered on May 07, 2023.

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.