International safety notice
90380 Ανάκληση της παρτίδας 160301 (ημ. ληξης 3/2019) του ιατροτεχνολογικού προϊόντος χειρουργικά ράμματα HDA SUTURES POLYGLYCOLIC ACID (Violet Braided Adsorbable suture 3/0 (2 metric) Για να δείτε την απόφαση πατήστε εδώ
Greece / EOF · GRC · Nov 25, 2016
Key facts
| Title | 90380 Ανάκληση της παρτίδας 160301 (ημ. ληξης 3/2019) του ιατροτεχνολογικού προϊόντος χειρουργικά ράμματα HDA SUTURES POLYGLYCOLIC ACID (Violet Braided Adsorbable suture 3/0 (2 metric) Για να δείτε την απόφαση πατήστε εδώ |
|---|---|
| Regulator | Greece / EOF |
| Country | GRC |
| Manufacturer | KALTEQ ΑΕ |
| Models | Γ.Π.ΟΙΚ.130648, 90380, 2106549500, 65475, 2132040540, 30-82009, ’ΑΡΙΘ.239-2016, 160301, Ν.1316, 2.9.2016, 243-2016 |
| Event type | Recall, Safety Notice |
| Date | Nov 25, 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