International safety notice

Equipment

Brazil / Anvisa · BRA · Oct 9, 2015

Key facts

Title Equipment
Regulator Brazil / Anvisa
Country BRA
Brand Infusomat Space Set Air IL (Non-photosensitive equipment for infusion of parenteral solutions in infusion pumps) - Code 441702SP - Registration 80136990755 Lots 15G21LA335, 15H21LA383, 15H21LA384, lSH24LA385 and 15H31lA398 and Equipment for Enteral Nutrition in Pumps of B.Braun Infusion (Infusomat Space Set Enteral Air) Code 402111SP - Registration number 80136990733, lot 15H2SLA388
Manufacturer DETENTOR DO REGISTRO NO BRASIL LABORATÓRIOS B BRAUN SA CNPJ 31673254000102 ENDEREÇO AV EUGÊNIO BORGES 1092 E AV JEQUITIBÁ 9 SÃO GONÇALO RIO DE JANEIRO TELEFONE 21 26023263
Models 441702SP, 402111SP, 15H21LA384, 15H2SLA388, lSH24LA385, 80136990733, 15G21LA335, 15H31lA398, 15H21LA383, 80136990755
Date Oct 9, 2015
Regulator page anvisa.gov.br

At a glance

  • No Recall
  • No Field safety notice
  • 1–9 Matching device models 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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