International safety notice

Kit Instrumental

Brazil / Anvisa · BRA · Nov 13, 2015

Key facts

Title Kit Instrumental
Regulator Brazil / Anvisa
Country BRA
Brand PFC AND SPECIALIST INSTRUMENTS (400mm Specialist 2 Intramedullary Rod Instrument (SP 2 IM) (PN 96-6120) ) - Registration nº 10132590285 - Lot: C4GA54, Lot: TBAGG, Lot: H0302, Lot: H0401, Lot: H0610, Lot : H0710, Lot: H0810, Lot: H1008, Lot: H0999
Manufacturer DETENTOR DO REGISTRO NO BRASIL JOHNSON JOHNSON DO BRASIL IND E COM DE PROD PARA SAÚDE LTDA CNPJ 54516661000101 ENDEREÇO RUA GERIVATIBA NO 207 SÃO PAULO SÃO PAULO TELEFONE 12 3932 1659 FABRICANTE DEPUY INTERNATIONAL LTD ST ANTHONY S ROAD LEEDS REINO UNIDO
Models H0610, H0302, 96-6120, H0810, H0999, 10132590285, C4GA54, H1008, H0401, H0710
Date Nov 13, 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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