International safety notice
Monitores multiparamétricos de paciente portátiles B20/B20i/B40/B40i (Bx0) y B105/B125 (B1x5)
Spain / AEMPS · ESP · Nov 12, 2018
Key facts
| Title | Monitores multiparamétricos de paciente portátiles B20/B20i/B40/B40i (Bx0) y B105/B125 (B1x5) |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Monitores multiparamétricos de paciente portátiles B20/B20i/B40/B40i (Bx0) y B105/B125 (B1x5) |
| Manufacturer | GE Medical Systems Information Technologies Inc., Estados Unidos (fabricante monitores B20/B40/B125/B105) y GE Healthcare Finland Oy, Finlandia (fabricante monitores B20i/B40i) |
| Models | 36132, 2018-587, 2026338-008, 2026339-007, 28023, 35-37, 53188, 2000716-013E, 902118226, 48584 |
| Event type | Safety Notice |
| Date | Nov 12, 2018 |
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