International safety notice
Teligen VR ICD
Swiss / SwissMedic · CHE · Sep 23, 2014
Key facts
| Title | Teligen VR ICD |
|---|---|
| Regulator | Swiss / SwissMedic |
| Country | CHE |
| Brand | Teligen VR ICD |
| Manufacturer | Cardiac Pacemaker Inc |
| Models | 002431, 016950, 000758, 004197, 000651, 1.800.CARDIAC, 004055, 000718, 000884, 52.000, 009581, 009624 and 194 more |
| Event type | Safety Notice |
| Date | Sep 23, 2014 |
| Regulator page | fsca.swissmedic.ch |
At a glance
- No Recall
- Yes Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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