International safety notice
Analizador de inmunoensayo DxI 9000 Access. Referencia: C11137. UDI-DI: 15099590732103
Spain / AEMPS · ESP · Jun 12, 2024
Key facts
| Title | Analizador de inmunoensayo DxI 9000 Access. Referencia: C11137. UDI-DI: 15099590732103 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Analizador de inmunoensayo DxI 9000 Access. Referencia: C11137. UDI-DI: 15099590732103 |
| Manufacturer | Beckman Coulter. EEUU. |
| Models | 300251, 300211, 300166, 300181, C11137, 300248, 300165, 300169, 300282, 300269, 300231, 300218 and 141 more |
| Event type | Safety Notice |
| Date | Jun 12, 2024 |
At a glance
- No Recall
- Yes Field safety notice
- 10–99 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