International safety notice

Technical name: M. de Cultura e Dispos.

Brazil / Anvisa · BRA · Oct 18, 2017

Key facts

Title Technical name: M. de Cultura e Dispos.
Regulator Brazil / Anvisa
Country BRA
Brand Commercial name: Family of Differentials for Ident. Technical name: M. de Cultura e Dispos. ANVISA registration number: 10158120571 Risk class: II Affected model: Not applicable. Affected serial numbers: 2420348103, 2420192403, 2420198203, 2420200103, 2420204103, 2420205103, 2420209203, 2420214403, 2420217203, 2420220 203, 2420226403, 2420229203, 2420239203, 2420243203, 2420247403, 2420248203, 2420253203, 2420261403, 2420267103, 2420282403, 2420289403, 2420290103, 2420296403, 2420300203, 2420302103, 2420303103, 2420307103, 2420309403, 2420314203, 2420317203, 2420317403, 2420320103, 2420321103, 2420322103, 2420330113, 2420331403, 2420352403, 2420353403
Manufacturer EMPRESA DETENTORA DO REGISTRO BIOMPERIEUX BRASIL IND E COM DE PROD LABORATORIAIS LTDA CNPJ 33040635000171 ESTRADA DO MAPUÁ 491 LOTE 1 TAQUARA RIO DE JANEIRO RJ FABRICANTE BIOMÉRIEUX INC 595 ANGLUM ROAD HAZELWOOD MISSOURI USA 63042 TELEFONE 33 4 78 87 76 67 EMAIL JEFFSCANLANBIOMERIEUXCOM
Models 2420290103, 2420217203, 2420314203, 2420321103, 2420289403, 2420302103, 2420309403, 2420353403, 2420243203, 2420209203, 2420307103, 2420200103 and 27 more
Date Oct 18, 2017
Regulator page anvisa.gov.br

At a glance

  • No Recall
  • No Field safety notice

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