International safety notice
Ανάκληση παρτίδας του in vitro διαγνωστικού ιατροτεχνολογικού προϊόντος "MDMulticard Basic Extended Phenotype" Για να δείτε την απόφαση πατήστε εδώ
Greece / EOF · GRC · Jun 25, 2018
Key facts
| Title | Ανάκληση παρτίδας του in vitro διαγνωστικού ιατροτεχνολογικού προϊόντος "MDMulticard Basic Extended Phenotype" Για να δείτε την απόφαση πατήστε εδώ |
|---|---|
| Regulator | Greece / EOF |
| Country | GRC |
| Manufacturer | Βαρελάς Α.Ε. |
| Models | 64580, 11-12-2017, 2106549500, 14-06-2018, 2132040527, 30-112018 |
| Event type | Recall, Safety Notice |
| Date | Jun 25, 2018 |
| 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