International safety notice

IMPLANT

Brazil / Anvisa · BRA · Feb 1, 2016

Key facts

Title IMPLANT
Regulator Brazil / Anvisa
Country BRA
Brand Knee Arthroplasty/Knee Prosthesis System;
Manufacturer DETENTOR DO REGISTRO DABASONS IMPORTAÇÃO EXPORTAÇÃO E COMÉRCIO LTDA ENDEREÇO RUA PEIXOTO GOMIDE 515 2 ANDAR SÃO PAULO SP CNPJ 61519955000144 FABRICANTE ZIMMER INC 1800 WEST CENTER STREET WARSAW INDIANA 46580 EUA
Models 62041405, 62103398, 6307-00-009, 62142201, 62156242, 6307-00-008, 62137144, 6307-00-006, 10099430107
Date Feb 1, 2016
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