International safety notice
Centricity Enterprise Archive, version de software: V2.X, V3.X, V4.X y Enterprise Archive, versión de software: 8.
Spain / AEMPS · ESP · Sep 29, 2023
Key facts
| Title | Centricity Enterprise Archive, version de software: V2.X, V3.X, V4.X y Enterprise Archive, versión de software: 8. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Centricity Enterprise Archive, version de software: V2.X, V3.X, V4.X y Enterprise Archive, versión de software: 8. |
| Manufacturer | GE Medical Systems, LLC, EEUU. |
| Models | 18446744073710726636, 28023, 35-37, RECALL.85469, 2023-458, V4.X.ENTERPRISE, 97909, 91.822.52.89, 28022, 85469 |
| Event type | Safety Notice |
| Date | Sep 29, 2023 |
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