International safety notice
Sistema CLINITEK Status®Connect: Analizador CLINITEK Status®+europeo, número de material 10379677, versión de software V2.620, junto con la Plataforma CLINITEK Status Connect, número de material 10376322, versión de software V2.4.2.0
Spain / AEMPS · ESP · Jul 22, 2020
Key facts
| Title | Sistema CLINITEK Status®Connect: Analizador CLINITEK Status®+europeo, número de material 10379677, versión de software V2.620, junto con la Plataforma CLINITEK Status Connect, número de material 10376322, versión de software V2.4.2.0 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Sistema CLINITEK Status®Connect: Analizador CLINITEK Status®+europeo, número de material 10379677, versión de software V2.620, junto con la Plataforma CLINITEK Status Connect, número de material 10376322, versión de software V2.4.2.0 |
| Manufacturer | Siemens Healthcare Diagnostics Manufacturing Ltd, Irlanda |
| Models | 10376322, 2020-100.LA, 10376323, V2.4.2.0, 10379681, 2020-412, 57954, 20-001.A.OUS, 28906, 28022, 0114786, 20-001.B.OUS and 16 more |
| Event type | Safety Notice |
| Date | Jul 22, 2020 |
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