International safety notice
Safety Notice: Instructions for Use Modification for VASOVIEW HEMOPRO Endoscopic Vessel Harvesting System, Maquet
Germany / BfArM · DEU · Feb 23, 2010
Key facts
| Title | Safety Notice: Instructions for Use Modification for VASOVIEW HEMOPRO Endoscopic Vessel Harvesting System, Maquet |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | VASOVIEW HEMOPRO Endoscopic Vessel Harvesting System, Maquet |
| Manufacturer | Safety Notice: Instructions for Use Modification for VASOVIEW HEMOPRO Endoscopic Vessel Harvesting System, Maquet |
| Models | 408-635-0600, 408.635.0700, 5.1.18, 95134, 5.1.19, VH-3000-W, MCV00001477 |
| Date | Feb 23, 2010 |
| 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