International safety notice
Advisory Notice from Guidant for the RX ACCUNETTM Embolic Protection System
Germany / BfArM · DEU · May 13, 2005
Key facts
| Title | Advisory Notice from Guidant for the RX ACCUNETTM Embolic Protection System |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the RX ACCUNETTM Embolic Protection System |
| Manufacturer | Advisory Notice from Guidant for the RX ACCUNETTM Embolic Protection System |
| Models | 92221222, 21222, 32221222, 202.5, 222.5, 200.5, DEATH2, —200.5, 0.014, 1-2EZ.S, 8TEPS |
| Date | May 13, 2005 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
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