International safety notice
Sistema implante coclear MAESTRO:SONATAti100 Standard,SONATAti100 HStandard,SONATAti100 FLEXsoft,Mi100 CONCERTO PIN+FLEX28,Mi1000 CONCERTO +FLEX28, Mi1000 CONCERTO +Standard,Mi1000 CONCERTO PIN+Standard,Mi1000 CONCERTO PIN+FLEXsoft,Mi1000 CONCERTO +Medium
Spain / AEMPS · ESP · Dec 7, 2018
Key facts
| Title | Sistema implante coclear MAESTRO:SONATAti100 Standard,SONATAti100 HStandard,SONATAti100 FLEXsoft,Mi100 CONCERTO PIN+FLEX28,Mi1000 CONCERTO +FLEX28, Mi1000 CONCERTO +Standard,Mi1000 CONCERTO PIN+Standard,Mi1000 CONCERTO PIN+FLEXsoft,Mi1000 CONCERTO +Medium |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Sistema implante coclear MAESTRO:SONATAti100 Standard,SONATAti100 HStandard,SONATAti100 FLEXsoft,Mi100 CONCERTO PIN+FLEX28,Mi1000 CONCERTO +FLEX28, Mi1000 CONCERTO +Standard,Mi1000 CONCERTO PIN+Standard,Mi1000 CONCERTO PIN+FLEXsoft,Mi1000 CONCERTO +Medium |
| Manufacturer | MED-EL Elektromedizinische Geraete GmbH, 6020 Innsbruck, Austria |
| Models | 07670, 07680, 164324, 04215, 07672, 147748, 28760, 223013, SONATATI100, 08842, 04210, 510079 and 26 more |
| Event type | Safety Notice |
| Date | Dec 7, 2018 |
At a glance
- No 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