International safety notice

Safety Notice for the Guide tube for segments and cervical sleeves, straight (a component of the Segmented Cervix Applicator set), Varian medical systems

Germany / BfArM · DEU · Oct 29, 2012

Key facts

Title Safety Notice for the Guide tube for segments and cervical sleeves, straight (a component of the Segmented Cervix Applicator set), Varian medical systems
Regulator Germany / BfArM
Country DEU
Brand segments and cervical sleeves, straight (a component of the Segmented Cervix Applicator set), Varian medical systems
Manufacturer Safety Notice for the Guide tube for segments and cervical sleeves, straight (a component of the Segmented Cervix Applicator set), Varian medical systems
Models 00531, 1293-542-626, GM11000960, 1-434-979-1540, 1-949-221-7631, 2012-10-15, H640764, $SSOLFDWRU6HWದ, &7&RPSDWLEOH05&RPSDWLELOLW\&RQGLWLRQDO, BT-00806, H600272, 06HJPHQWHG&HUYL and 16 more
Date Oct 29, 2012
Regulator page bfarm.de

At a glance

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