International safety notice

Mo.Ma Ultra 9F 013. Referencia: MOM0130069X6.

Spain / AEMPS · ESP · Oct 23, 2023

Key facts

Title Mo.Ma Ultra 9F 013. Referencia: MOM0130069X6.
Regulator Spain / AEMPS
Country ESP
Brand Mo.Ma Ultra 9F 013. Referencia: MOM0130069X6.
Manufacturer Medtronic, Inc., EEUU.
Models 226388209, 28022, 226403314, LOTE226373365, US-MF-000019977, PCPDMO.MA.ULTRA8F, 28050, PCPDMO.MA.ULTRA9F, MO.MA.ULTRA9F, 226373365, MOM0130068X5, 98877 and 6 more
Event type Safety Notice
Date Oct 23, 2023

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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