International safety notice

Corrective action for the product astraia software for women’s health, astraia software gmbh

Germany / BfArM · DEU · Jun 3, 2015

Key facts

Title Corrective action for the product astraia software for women’s health, astraia software gmbh
Regulator Germany / BfArM
Country DEU
Brand women’s health, astraia software gmbh
Manufacturer Corrective action for the product astraia software for women’s health, astraia software gmbh
Models 127114712, 22.5.2015, 1.24.X, 1.22.X, 1.20.X, 1.23.X, AST-4018, 1.21.X, 80804
Date Jun 3, 2015
Regulator page bfarm.de

At a glance

  • No Recall
  • No Field safety notice

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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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