International safety notice

Alert 2487 (Technosurveillance) - Boston - Uphold Vaginal Support;

Brazil / Anvisa · BRA · Feb 22, 2018

Key facts

Title Alert 2487 (Technosurveillance) - Boston - Uphold Vaginal Support;
Regulator Brazil / Anvisa
Country BRA
Brand Trade name: Uphold Vaginal Support Technical name: Screens ANVISA registration number: 10341350701 Risk class: III Affected model: M0068317080 Commercial name: Capio Suture Capture Device Technical name: Suture Passer ANVISA registration number: 10341350717 Risk class: II Affected model: M0068311251 Trade name: Capio SLIM - Suture Capture Device Technical name: Suture Passer ANVISA registration number: 10341350777 Risk class: II Affected model: M0068318250 Trade name: Uphold Lite with Capio SLIM - Vaginal Support System Technical name: Screen ANVISA registration number: 10341350779 Risk class: III Affected model: M0068318170
Manufacturer EMPRESA DETENTORA DO REGISTRO BOSTON SCIENTIFIC DO BRASIL LTDA CNPJ 01513946000114 AV DAS NAÇÕES UNIDAS 21476 EDIFÍCIOS P8 P9 E P10 VILA ALMEIDA SÃO PAULO SP FABRICANTE MEDVENTURE TECHNOLOGY CORPORATION 2301 CENTENNIAL BOULEVARD ESTADOS UNIDOS EMAIL REGULATORIOBSCICOM
Models 10341350779, M0068318250, 10341350701, M0068311251, 10341350777, 10341350717, M0068318170, M0068317080
Date Feb 22, 2018
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

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