International safety notice

Analizador de sedimento de orina Atellica® UAS 800. Nº material de Siemens 11065004 Sistema de análisis de orina automatizado Atellica® 1500.

Spain / AEMPS · ESP · Mar 1, 2022

Key facts

Title Analizador de sedimento de orina Atellica® UAS 800. Nº material de Siemens 11065004 Sistema de análisis de orina automatizado Atellica® 1500.
Regulator Spain / AEMPS
Country ESP
Brand Analizador de sedimento de orina Atellica® UAS 800. Nº material de Siemens 11065004 Sistema de análisis de orina automatizado Atellica® 1500.
Manufacturer Siemens Healthcare Diagnostics Inc., EE.UU.
Models 800SISTEMA, 28022, 77597, 91.822.52.89, 28906, 2022-105, 11065004
Event type Safety Notice
Date Mar 1, 2022

At a glance

  • No Recall
  • Yes Field safety notice
  • 1–9 Matching device models in FDA data
  • 1–9 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