International safety notice
Safety Notice for the Intuitive Surgical 5mm Curved Cannula for Single-Site™ Instruments used with the da Vinci® Si™ Surgical System, Intuitive Surgical
Germany / BfArM · DEU · Apr 23, 2014
Key facts
| Title | Safety Notice for the Intuitive Surgical 5mm Curved Cannula for Single-Site™ Instruments used with the da Vinci® Si™ Surgical System, Intuitive Surgical |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Single-Site™ Instruments used with the da Vinci® Si™ Surgical System, Intuitive Surgical |
| Manufacturer | Safety Notice for the Intuitive Surgical 5mm Curved Cannula for Single-Site™ Instruments used with the da Vinci® Si™ Surgical System, Intuitive Surgical |
| Models | VE123005, VE123104, VE121904, VE122606, 2955842-02-28-2014-001-R, VE113402, VE121002, VE120902, 716-3040, VE121004, VE122901, VE121402 and 126 more |
| Date | Apr 23, 2014 |
| 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