International safety notice

A.Π. 57246 Ανάκληση του ιατροτεχνολογικού προϊόντος (Αperto Eterna LT) Για να δείτε την απόφαση πατήστε εδώ.

Greece / EOF · GRC · Sep 15, 2015

Key facts

Title A.Π. 57246 Ανάκληση του ιατροτεχνολογικού προϊόντος (Αperto Eterna LT) Για να δείτε την απόφαση πατήστε εδώ.
Regulator Greece / EOF
Country GRC
Models 57246, V2.1A, 2040435, 01-09-2015, 30-8-2009, Ν.1316, ΔΥΓ8Δ, 6549500, Γ.Π.ΟΙΚ.130648
Event type Recall, Safety Notice
Date Sep 15, 2015
Regulator page eof.gr

At a glance

  • Yes Recall
  • Yes 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

Browse all International device safety notices