International safety notice

Sistema de embolización líquido PHIL™ (Líquido inyectable hidrófobo precipitante) Números de catálogo LEN10250, LEN1025RE, LEN10300, LEN10300RE, LEN10350, LEN10350RE, LEN10LV250, LEN10LV250RE

Spain / AEMPS · ESP · Feb 18, 2021

Key facts

Title Sistema de embolización líquido PHIL™ (Líquido inyectable hidrófobo precipitante) Números de catálogo LEN10250, LEN1025RE, LEN10300, LEN10300RE, LEN10350, LEN10350RE, LEN10LV250, LEN10LV250RE
Regulator Spain / AEMPS
Country ESP
Brand Sistema de embolización líquido PHIL™ (Líquido inyectable hidrófobo precipitante) Números de catálogo LEN10250, LEN1025RE, LEN10300, LEN10300RE, LEN10350, LEN10350RE, LEN10LV250, LEN10LV250RE
Manufacturer MICROVENTION INC., Estados Unidos
Models 19080513A, 19110614H, LEN10300RE, 20070912E, 0100842429101568, 20032511T, 2002181DG, 20070111Y, 19090311Z, 191106135, 190121124, 19092311E and 106 more
Event type Safety Notice
Date Feb 18, 2021

At a glance

  • No Recall
  • Yes Field safety notice

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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