International safety notice
Dispositivo de respiración artificial de emergencia y de transporte MEDUMAT Standard²
Spain / AEMPS · ESP · Aug 11, 2020
Key facts
| Title | Dispositivo de respiración artificial de emergencia y de transporte MEDUMAT Standard² |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Dispositivo de respiración artificial de emergencia y de transporte MEDUMAT Standard² |
| Manufacturer | WEINMANN Emergency Medical Technology GmbH + Co. KG, Alemania. |
| Models | 115967, DE288367727, 22770, STANDARD², 13485, 2020-468, DE35ZZZ00000353971, 24558, 96-0F, 28022, 61132, SOFTWARE4.13 and 12 more |
| Event type | Safety Notice |
| Date | Aug 11, 2020 |
At a glance
- No Recall
- Yes Field safety notice
- 10–99 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