International safety notice

EOlife®, ref. A0000055 y EOlife® Premium Pack, ref.A0000060.

Spain / AEMPS · ESP · Mar 30, 2022

Key facts

Title EOlife®, ref. A0000055 y EOlife® Premium Pack, ref.A0000060.
Regulator Spain / AEMPS
Country ESP
Brand EOlife®, ref. A0000055 y EOlife® Premium Pack, ref.A0000060.
Manufacturer Archeon, Francia.
Models 28823, FSCA-2022-N°01, 28022, LOTEF201000140, FSN-2022-N°01, A0000055.EOLIFE®, A0000055, 78187, 1000M, 91.822.52.89, A0000060, 2022-157 and 5 more
Event type Safety Notice
Date Mar 30, 2022

At a glance

  • No Recall
  • Yes Field safety notice
  • 100–999 Matching device models in FDA data
  • 100–999 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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