International safety notice
Ανάκληση των Ιατροτεχνολογικών προϊόντων Pipeline embolization Device (Pipeline classic), Alligator Retrieval Device, Marathon flow Directed Microcatheter (με στυλεό), UltraFlow HPC Flow Directed Microcatheter (με στυλεό) και Xcelerator Hydrophilic Guidewire Για να δείτε την απόφαση πατήστε εδώ
Greece / EOF · GRC · Oct 24, 2016
Key facts
| Title | Ανάκληση των Ιατροτεχνολογικών προϊόντων Pipeline embolization Device (Pipeline classic), Alligator Retrieval Device, Marathon flow Directed Microcatheter (με στυλεό), UltraFlow HPC Flow Directed Microcatheter (με στυλεό) και Xcelerator Hydrophilic Guidewire Για να δείτε την απόφαση πατήστε εδώ |
|---|---|
| Regulator | Greece / EOF |
| Country | GRC |
| Manufacturer | ΥΓΕΙΑΣΗ ΑΕ |
| Models | 12.10.2016, 13.10.2016, 75254, 75360, 74804, Ν.1316, 30-8-2009, Γ.Π.ΟΙΚ.130648, 2106549500, Ν.3730, 2132040540 |
| Event type | Recall, Safety Notice |
| Date | Oct 24, 2016 |
| Regulator page | eof.gr |
At a glance
- Yes Recall
- Yes 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