International safety notice
UniCel DxC 600, UniCel DxC 600 PRO, UniCel DxC 600i, UniCel DxC 680i, UniCel DxC 660i
Swiss / SwissMedic · CHE · Nov 29, 2010
Key facts
| Title | UniCel DxC 600, UniCel DxC 600 PRO, UniCel DxC 600i, UniCel DxC 680i, UniCel DxC 660i |
|---|---|
| Regulator | Swiss / SwissMedic |
| Country | CHE |
| Brand | UniCel DxC 600, UniCel DxC 600 PRO, UniCel DxC 600i, UniCel DxC 680i, UniCel DxC 660i |
| Manufacturer | Beckman Coulter Inc. |
| Models | Gefaf1, DE205538094, 657133, 333-633, B00815AA, regelmaf1igen, folgendermaf1en, D-47807, 0-47704, dar0ber, 57994362, 7879-2 and 22 more |
| Event type | Safety Notice |
| Date | Nov 29, 2010 |
| Regulator page | fsca.swissmedic.ch |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 Matching device models 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