International safety notice
CARESCAPE PDM (Patient Data Module) con tecnología Masimo SET® SpO2. Ver referencias afectadas de CARESCAPE PDM, medios de software y unidades de reemplazo de campo (FRU) en la nota de aviso de la empresa
Spain / AEMPS · ESP · Jul 13, 2021
Key facts
| Title | CARESCAPE PDM (Patient Data Module) con tecnología Masimo SET® SpO2. Ver referencias afectadas de CARESCAPE PDM, medios de software y unidades de reemplazo de campo (FRU) en la nota de aviso de la empresa |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | CARESCAPE PDM (Patient Data Module) con tecnología Masimo SET® SpO2. Ver referencias afectadas de CARESCAPE PDM, medios de software y unidades de reemplazo de campo (FRU) en la nota de aviso de la empresa |
| Manufacturer | GE Medical Systems Information Technologies Inc., Estados Unidos |
| Models | 00840682110440, 28022, 2034826-004, 91.822.52.89, 18004, 902118226, 2034826-012, 2031069-010, 2045825-001, 2094504-001, 2045825-002, SPO2VER and 24 more |
| Event type | Safety Notice |
| Date | Jul 13, 2021 |
At a glance
- No Recall
- Yes Field safety notice
- 10–99 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