International safety notice
Ambu® VivaSight 2 Kit DLT 35 Fr; Referencia: 412351000 • Ambu® VivaSight 2 Kit DLT 37 Fr; Referencia: 412371000 • Ambu® VivaSight 2 Kit DLT 39 Fr; Referencia: 412391000 • Ambu® VivaSight 2 Kit DLT 41 Fr; Referencia: 412411000
Spain / AEMPS · ESP · Jun 13, 2022
Key facts
| Title | Ambu® VivaSight 2 Kit DLT 35 Fr; Referencia: 412351000 • Ambu® VivaSight 2 Kit DLT 37 Fr; Referencia: 412371000 • Ambu® VivaSight 2 Kit DLT 39 Fr; Referencia: 412391000 • Ambu® VivaSight 2 Kit DLT 41 Fr; Referencia: 412411000 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Ambu® VivaSight 2 Kit DLT 35 Fr; Referencia: 412351000 • Ambu® VivaSight 2 Kit DLT 37 Fr; Referencia: 412371000 • Ambu® VivaSight 2 Kit DLT 39 Fr; Referencia: 412391000 • Ambu® VivaSight 2 Kit DLT 41 Fr; Referencia: 412411000 |
| Manufacturer | Ambu A/S, Dinamarca |
| Models | 80476, DK-MF-000001437, 28027, 412411000, 261-265, 91.822.52.89, 412371000AMBU®, 412371000, 412391000AMBU®, 2022-295, 412351000AMBU®, 412351000 and 2 more |
| Event type | Safety Notice |
| Date | Jun 13, 2022 |
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