International safety notice
Programador LATITUDE®, Modelo 3300
Spain / AEMPS · ESP · Sep 20, 2018
Key facts
| Title | Programador LATITUDE®, Modelo 3300 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Programador LATITUDE®, Modelo 3300 |
| Manufacturer | Cardiac Pacemaker Inc., EEUU. (Subsidiaria de propiedad absoluta de Guidant Corporation y de Boston Scientific Corporation) |
| Models | 28042, 00802526597206, 2018-490, 47787, 91.822.52.89, 49LJ9PK824, 28022, 92287323-FA, 00802526585005, 623300-200, 623300-100 |
| Event type | Safety Notice |
| Date | Sep 20, 2018 |
At a glance
- No Recall
- Yes 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