International safety notice
Urgent Field Safety Notice about a change to the instructions for use/ user's manual regarding the defibrillators Paramedic CU-ER1, CU-ER2, CU-ER3 and CU-ER5, CU Medical Systems
Germany / BfArM · DEU · Oct 6, 2010
Key facts
| Title | Urgent Field Safety Notice about a change to the instructions for use/ user's manual regarding the defibrillators Paramedic CU-ER1, CU-ER2, CU-ER3 and CU-ER5, CU Medical Systems |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | use/ user's manual regarding the defibrillators Paramedic CU-ER1, CU-ER2, CU-ER3 and CU-ER5, CU Medical Systems |
| Manufacturer | Urgent Field Safety Notice about a change to the instructions for use/ user's manual regarding the defibrillators Paramedic CU-ER1, CU-ER2, CU-ER3 and CU-ER5, CU Medical Systems |
| Models | LJE3561, 2010-002, 2.1.3, 60601-2.4, CU-ER2, 2.1.2, CAR-DI-2010-002, 3.1.3, 220-878, 6.2.1, 1647-1, CU-ER3 and 13 more |
| Date | Oct 6, 2010 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No 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