International safety notice
Ανάκληση παρτίδων του Ιατροτεχνολογικού προϊόντος Twin-Pass Για να δείτε την απόφαση πατήστε εδώ
Greece / EOF · GRC · Oct 6, 2016
Key facts
| Title | Ανάκληση παρτίδων του Ιατροτεχνολογικού προϊόντος Twin-Pass Για να δείτε την απόφαση πατήστε εδώ |
|---|---|
| Regulator | Greece / EOF |
| Country | GRC |
| Manufacturer | Μ.Σ.ΙΑΚΩΒΙΔΗΣ ΕΛΛΑΣ ΑΕ |
| Models | 582580, 596936, 593695, 589884, 592920, Ν.1316, 586399, 570787, Ν.3730, Γ.Π.ΟΙΚ.130648, 2132040540, 30-8-2009 and 7 more |
| Event type | Recall, Safety Notice |
| Date | Oct 6, 2016 |
| Regulator page | eof.gr |
At a glance
- Yes Recall
- Yes Field safety notice
- 1–9 Matching device models 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