International safety notice

Technical name: Cannulas, Surgical Instruments, Non-rigid, non-absorbable fixation system for osteosynthesis, Non-absorbable screw for osteosynthesis

Brazil / Anvisa · BRA · May 24, 2017

Key facts

Title Technical name: Cannulas, Surgical Instruments, Non-rigid, non-absorbable fixation system for osteosynthesis, Non-absorbable screw for osteosynthesis
Regulator Brazil / Anvisa
Country BRA
Brand Trade name: Cannulas, Surgical Instruments, Non-rigid, non-absorbable fixation system for osteosynthesis, Non-absorbable screw for osteosynthesis Technical name: Cannulas, Surgical Instruments, Non-rigid, non-absorbable fixation system for osteosynthesis, Non-absorbable screw for osteosynthesis Number of ANVISA registration: 80044680043, 80044680047, 80044680052, 80044680144, 80044680164 Risk class: III Affected model: 900360, 908520, 24616, 14-400436, 900363H, 9 08518 Affected serial numbers: 606770, 579290, 579300, 606160, 664740, 565910, 675890
Manufacturer EMPRESA DETENTORA DO REGISTRO BIOMET 3I DO BRASIL COMÉRCIO DE APARELHOS MÉDICOS LTDA CNPJ 02913684000148 ENDEREÇO RUA MACHADO BITTENCOURT 361 12º ANDAR SÃO PAULO SP 11 35681300 FABRICANTE BIOMET INC 56 EAST BELL DRIVE WARSAW IN ESTADOS UNIDOS
Models 908520, 606160, 80044680052, 80044680047, 675890, 80044680043, 14-400436, 565910, 579290, 606770, 900363H, 664740 and 6 more
Date May 24, 2017
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

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