International safety notice
Desfibriladores automáticos implantables subcutáneos (S-ICD) EMBLEM™ (Modelos A209 y A219) y Electrodo subcutáneo S-ICD EMBLEM modelo 3501
Spain / AEMPS · ESP · Dec 11, 2020
Key facts
| Title | Desfibriladores automáticos implantables subcutáneos (S-ICD) EMBLEM™ (Modelos A209 y A219) y Electrodo subcutáneo S-ICD EMBLEM modelo 3501 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Desfibriladores automáticos implantables subcutáneos (S-ICD) EMBLEM™ (Modelos A209 y A219) y Electrodo subcutáneo S-ICD EMBLEM modelo 3501 |
| Manufacturer | Cardiac Pacemaker Inc (Boston Scientific Corporation), EEUU |
| Models | 92384167, 00802526544101, 2018.DESFIBRILADORES-CARDIOVERSORES, 00802526575204, 3IBIB, TRANSVENOSOS3, 2019-480, 3.350, 64017, 92400926D, 00802526590436, 00802526575228 and 55 more |
| Event type | Safety Notice |
| Date | Dec 11, 2020 |
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