International safety notice

Equipo de cateterismo arterial

Spain / AEMPS · ESP · Jul 19, 2019

Key facts

Title Equipo de cateterismo arterial
Regulator Spain / AEMPS
Country ESP
Brand Equipo de cateterismo arterial
Manufacturer Teleflex Medical , Irlanda.
Models DE-00820-MKHS, 71F19C1651, 71F19C1025, 71F19C1529, 71F19C0818, 91.822.52.89, 71F19C0971, DE-00820-UB, 71F19C2023, 71F19B0185, 71F19C0463, SAC-00524 and 54 more
Event type Safety Notice
Date Jul 19, 2019

At a glance

  • No Recall
  • Yes Field safety notice
  • 1–9 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

Browse all International device safety notices