International safety notice
Ανάκληση του Ιατροτεχνολογικού προϊόντος AFX Endovascular AAA System των τύπων AFX device with Strata Graft material και AFX2 device in 28 mm Main Body and/or 20 mm Iliac Limbs Για να δείτε την απόφαση πατήστε εδώ
Greece / EOF · GRC · Feb 3, 2017
Key facts
| Title | Ανάκληση του Ιατροτεχνολογικού προϊόντος AFX Endovascular AAA System των τύπων AFX device with Strata Graft material και AFX2 device in 28 mm Main Body and/or 20 mm Iliac Limbs Για να δείτε την απόφαση πατήστε εδώ |
|---|---|
| Regulator | Greece / EOF |
| Country | GRC |
| Manufacturer | Plus Medica ΑΕ |
| Models | 6549500, Γ.Π.ΟΙΚ.130648, 2040365, 2-10-2009, 16-1-2017 |
| Event type | Recall, Safety Notice |
| Date | Feb 3, 2017 |
| 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