International safety notice
Analizador de sedimento de orina Atellica UAS 800 y sistema de análisis de orina automatizado Atellica 1500. Número de material de Siemens 11065004. UDI-DI: 00630414001357
Spain / AEMPS · ESP · Feb 21, 2024
Key facts
| Title | Analizador de sedimento de orina Atellica UAS 800 y sistema de análisis de orina automatizado Atellica 1500. Número de material de Siemens 11065004. UDI-DI: 00630414001357 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Analizador de sedimento de orina Atellica UAS 800 y sistema de análisis de orina automatizado Atellica 1500. Número de material de Siemens 11065004. UDI-DI: 00630414001357 |
| Manufacturer | Siemens Healthcare Diagnostics Inc, EEUU. |
| Models | 800SISTEMA, 91.822.52.89, 2024-083, 28043, 00630414001357, V4.0.400, 1500.NÚMERO, 28022, 102346, 11065004 |
| Event type | Safety Notice |
| Date | Feb 21, 2024 |
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