International safety notice

Technical Name: Endoscopy Accessories

Brazil / Anvisa · BRA · Mar 3, 2016

Key facts

Title Technical Name: Endoscopy Accessories
Regulator Brazil / Anvisa
Country BRA
Brand VIDEODUODENOSCOPE, model TJF-Q180V, registration 80124630021, risk class II, various batches/series 2101238, 2101449, 2101548, 2101553, 2101599, 2101631, 2101831, 2202550, 2 202634, 2203238, 2203353, 2203354, 2203356, 2303564, 2303904, 2303905 ,2303982,2304251,2304261,2304485,2304500,2404994,2405413,2405415,2405420,2405423,2405753,2505982,2505997,25 06057, 2001123, 2101369, 2101345, 2101598, 2101600, 2404998, 2505898, 2505892, 2506636, 2506609, 2507086 , 2507076, 2507023, 2506640, 2507137, 2507120, 2507134, 2507122.
Manufacturer DETENTOR DO REGISTRO OLYMPUS OPTICAL DO BRASIL LTDA ENDEREÇO RUA DO RÓCIO 4302º ANDARVILA OLÍMPIA SÃO PAULOSP FABRICANTE OLYMPUS MEDICAL SYSTEMS CORP ENDEREÇO 2951 ISHIKAWACHO HACHIOJISHI TÓQUIOJAPÃO
Models 2505898, 2101631, 2304485, 2507134, 2101548, 2506640, 2405753, 2505997, 2506636, 2304261, 2101831, 2203354 and 38 more
Date Mar 3, 2016
Regulator page anvisa.gov.br

At a glance

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