International safety notice

REAGENTS, ANTIBODY TO HUMAN IMMUNODEFICIENCY VIRUS REAGENTS, IMMUNOASSAY ENZYME REAGENTS, FLUORESCENCE IMMUNOASSAY

Brazil / Anvisa · BRA · Oct 27, 2000

Key facts

Title REAGENTS, ANTIBODY TO HUMAN IMMUNODEFICIENCY VIRUS REAGENTS, IMMUNOASSAY ENZYME REAGENTS, FLUORESCENCE IMMUNOASSAY
Regulator Brazil / Anvisa
Country BRA
Brand ABBOTT/MUREX DISPOSABLE TESTS FOR HUMAN IMMUNODEFICIENCY VIRUS 1 DIAGNOSTIC SYSTEM
Manufacturer ABBOTT LABORATORIES DIAGNOSTIC DIV 103243 100 ABBOTT PARK RD ABBOTT PARK IL 600646092
Date Oct 27, 2000
Regulator page anvisa.gov.br

At a glance

  • No Recall
  • No Field safety notice
  • 1–9 Matching device models in FDA data

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About International device safety notices

Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.

Source: National medical device regulators (as listed), compiled by Orca1

Browse all International device safety notices