International safety notice

Revocation of the Safety Alert on the sale of non-surgical procedure gloves without a conformity seal Disposable Non Woven Imp.

Brazil / Anvisa · BRA · Dec 28, 2010

Key facts

Title Revocation of the Safety Alert on the sale of non-surgical procedure gloves without a conformity seal Disposable Non Woven Imp.
Regulator Brazil / Anvisa
Country BRA
Brand GLOVE FOR SURGICAL PROCEDURE WITH LAGROTTA AZZURRA POWDER - Registered with Anvisa under number 80044540022 - all lots.
Manufacturer DETENTOR DO REGISTRO DO PRODUTO NO BRASIL DESCARTÁVEIS NON WOVEN IMPORTAÇÃO E EXPORTAÇÃO LTDA RUA FRANCISCO ASSIS GARRIDO 75 BLOCO B JARDIM SÃO LUIZ SÃO PAULOSP FONE 1152533333 RAMAL 3357 LAGROTTALAGROTTACOMBR
Models 80044540022
Date Dec 28, 2010
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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