International safety notice
Módulos de Datos del Paciente (PDM) Utilizados con los monitores CARESCAPE B450/B650/B850, SOLAR 8000M/I y Transport Pro.
Spain / AEMPS · ESP · Jun 16, 2020
Key facts
| Title | Módulos de Datos del Paciente (PDM) Utilizados con los monitores CARESCAPE B450/B650/B850, SOLAR 8000M/I y Transport Pro. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Módulos de Datos del Paciente (PDM) Utilizados con los monitores CARESCAPE B450/B650/B850, SOLAR 8000M/I y Transport Pro. |
| Manufacturer | GE Medical Systems Information Technologies, Inc., EEUU. |
| Models | 35-37, 2042084-001, 2034826-011, SOFTWAREV2.6, 00840682110440, 53188, 2034826-012, 2031069-010, 28023, 28022, V2.7.INCLUYE, 2020-335 and 6 more |
| Event type | Safety Notice |
| Date | Jun 16, 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