International safety notice

Technical Name: Catheters

Brazil / Anvisa · BRA · Apr 4, 2016

Key facts

Title Technical Name: Catheters
Regulator Brazil / Anvisa
Country BRA
Brand Trade name: DISPOSABLE INTRA AORTIC BALLOON CATHETER ## ANVISA registration number: 10216830016 ## Risk class: IV ## Affected model(s): IAB-S730C ## Lot(s) / Serial number(s) ) affected: 18F14A0041 18F14G0077 18F14C0003 18F14H0011 18F14C0006 18F15B0023 18F14C0021 18F15C0001 18F14C0026 18F15C0008 18F14C 0027 18F15C0026 18F14C0028 18F14E0039 18F14E0055 18F14E0058 18F14F0038 18F14G0057 ## DISTRIBUTION MAP ATTACHED
Manufacturer DADOS DO DETENTOR DO REGISTRO NO BRASIL GABMED PRODUTOS ESPECÍFICOS LTDA CNPJ 68867522000129 ENDEREÇO RUA ANTONIO DAS CHAGAS 966 CHÁCARA SANTO ANTONIO CEP 04714001 11 5182 3391SÃO PAULOSP DADOS DO FABRICANTE ARROW INTERNATIONAL INC 9 PLYMOUTH STREET EVERETTMA 02149
Models 18F14C0006, 18F14C0026, 18F15C0026, 18F14C0003, IAB-S730C, 18F14G0077, 18F14G0057, 18F14C0028, 18F15B0023, 18F15C0008, 18F14C0021, 18F14C0027 and 8 more
Date Apr 4, 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

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