International safety notice

Implantable screws

Brazil / Anvisa · BRA · Dec 30, 2015

Key facts

Title Implantable screws
Regulator Brazil / Anvisa
Country BRA
Brand TITE ORTHOFIX OSTEO SCREW;
Manufacturer DETENTOR DO REGISTRO ORTHOFIX DO BRASIL LTDA 02690906000100 RUA ALVES GUIMARÃES 1216 PINHEIROS SÃO PAULO SP CEP 05410002 11 30872266 FABRICANTE ORTHOFIX SRL VIA DELLE NAZIONI 937012 BUSSOLENGO VERONA ITÁLIA
Models 99-60139, 10392060062, 99-60138, R1406979, V1407156, 99-60103, V1409882, V1409048, V1407169, 99-60148, V1407155, 99-60100 and 7 more
Date Dec 30, 2015
Regulator page anvisa.gov.br

At a glance

  • No Recall
  • No Field safety notice
  • 10–99 Matching device models in FDA data
  • 10–99 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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