International safety notice

ImplanteImplantes EIT: Cajas cervicales Cellular Titanium® y Cajas lumbares Cellular Titanium® (PLIF y TLIF)

Spain / AEMPS · ESP · Nov 28, 2019

Key facts

Title ImplanteImplantes EIT: Cajas cervicales Cellular Titanium® y Cajas lumbares Cellular Titanium® (PLIF y TLIF)
Regulator Spain / AEMPS
Country ESP
Brand ImplanteImplantes EIT: Cajas cervicales Cellular Titanium® y Cajas lumbares Cellular Titanium® (PLIF y TLIF)
Manufacturer Emerging Implant Technologies GmbH (EIT), Alemania
Models D-78573, 28022, 55967, 2019-641, 91.822.52.89, 28938
Event type Safety Notice
Date Nov 28, 2019

At a glance

  • No Recall
  • Yes 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

Browse all International device safety notices