International safety notice

Absorbable Hemostats.

Brazil / Anvisa · BRA · Jul 2, 2013

Key facts

Title Absorbable Hemostats.
Regulator Brazil / Anvisa
Country BRA
Brand BIOMEND ORGANIC PATCH, BIOMEND and BIOMEND EXTEND models (Anvisa Registration: 10355870093. Affected lots: 1105175, 1111859 and 1104847 (Biomend Extend); 1111358 and 1111865 (Biomend). COLLA ORGANIC PATCH, COTE models, PLUG and TAPE (Anvisa Registration: 10355870152 ).Affected lots: 1110239 (Colla Plug), 1111644 (Colla Cote) and 1112262 (Colla Tape. See details in the attachment http://portal.anvisa.gov.br/wps/wcm/connect/e73bf38040357a1cb017f0dc5a12ff52/Alerta_Biomend.pdf? MOD=AJPERES
Manufacturer DETENTOR DO REGISTRO BIOMÉDICA EQUIPAMENTOS E SUPRIMENTOS HOSPITALARES LTDA CNPJ 01299509000140
Models 1112262, 1105175, 1111358, 1111865, 10355870152, 1111859, 10355870093, e73bf38040357a1cb017f0dc5a12ff52, 1104847, 1111644, 1110239
Date Jul 2, 2013
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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