International safety notice

Alert 2873 (Technosurveillance) - Olympus Optical do Brasil Ltda.

Brazil / Anvisa · BRA · May 9, 2019

Key facts

Title Alert 2873 (Technosurveillance) - Olympus Optical do Brasil Ltda.
Regulator Brazil / Anvisa
Country BRA
Brand Commercial Name: Sterile Aspiration Valve (part of the Broncofibroscopio product) Technical Name: Flexible Endoscope ANVISA registration number: 80124630018 Risk Class: II Affected model: MAJ-209 Affected serial numbers: 89H/8ZH
Manufacturer EMPRESA DETENTORA DO REGISTRO OLYMPUS OPTICAL DO BRASIL LTDA CNPJ 04937243000101 RUA DO RÓCIO 430 2º ANDAR VILA OLÍMPIA SÃO PAULO SP TEL 30466400 RAMAL 6465 EMAIL QUALIDADEBRASILOLYMPUSCOM FABRICANTE DO PRODUTO OLYMPUS MEDICAL SYSTEMS CORP 2951 ISHIKAWA CHO HACHIOJISHI TÓQUIO JAPÃO
Models 80124630018, MAJ-209
Date May 9, 2019
Regulator page anvisa.gov.br

At a glance

  • No Recall
  • No Field safety notice
  • 10–99 Matching device models in FDA data
  • 10–99 Matching catalog numbers 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