International safety notice
Ανάκληση των παρτίδων 507133502 & 608177603 του ιατροτεχνολογικού προϊόντος “ DERMAGRIP Ultra LS Nitrile Examination Gloves – Powder Free – Μedium χωρίς πούδρα – Medium & Large” Για να δείτε την απόφαση πατήστε εδώ
Greece / EOF · GRC · Jul 10, 2017
Key facts
| Title | Ανάκληση των παρτίδων 507133502 & 608177603 του ιατροτεχνολογικού προϊόντος “ DERMAGRIP Ultra LS Nitrile Examination Gloves – Powder Free – Μedium χωρίς πούδρα – Medium & Large” Για να δείτε την απόφαση πατήστε εδώ |
|---|---|
| Regulator | Greece / EOF |
| Country | GRC |
| Manufacturer | στην Ελλάδα: MILONAS ΗΕΑLTH A.E. ΙΑΤΡΙΚΑ ΠΡΟΪΟΝΤΑ Κατασκευαστής : W RP ASIA Pacific Sdn Bhd - MALAYSIA |
| Models | 2040435, 61293, 07-2021, 608177603, 52-2017, Ν.1316, 6549500, 06-2020, 507133502, 51-2017 |
| Event type | Recall, Safety Notice |
| Date | Jul 10, 2017 |
| Regulator page | eof.gr |
At a glance
- Yes Recall
- Yes Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 Matching catalog numbers 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