International safety notice

Mesa QF VE en los sistemas: ARTIS pheno, UDI-DI 4056869046877 ARTIS icono biplane, UDI-DI 4056869063317 ARTIS icono floor, UDI-DI 4056869149325

Spain / AEMPS · ESP · Dec 22, 2023

Key facts

Title Mesa QF VE en los sistemas: ARTIS pheno, UDI-DI 4056869046877 ARTIS icono biplane, UDI-DI 4056869063317 ARTIS icono floor, UDI-DI 4056869149325
Regulator Spain / AEMPS
Country ESP
Brand Mesa QF VE en los sistemas: ARTIS pheno, UDI-DI 4056869046877 ARTIS icono biplane, UDI-DI 4056869063317 ARTIS icono floor, UDI-DI 4056869149325
Manufacturer Siemens Healthcare GmbH, Alemania.
Models ANAL6GICO, PRESI6N, ANTICOLISI6N, LEGISLACI6N, ANGULACI6N, 4056869149325, REF.1, 4056869046877, DESCRIPCI6N, DISTRIBUCI6N, §1020.32, M004RH20010 and 179 more
Event type Safety Notice
Date Dec 22, 2023

At a glance

  • No Recall
  • Yes Field safety notice
  • 100–999 Matching device models in FDA data
  • 10–99 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