International safety notice
Tubo endotraqueal resistencia al laser, LaserTube. Ver referencias afectadas en el anexo 2 de la nota de aviso empresa.
Spain / AEMPS · ESP · Jul 2, 2020
Key facts
| Title | Tubo endotraqueal resistencia al laser, LaserTube. Ver referencias afectadas en el anexo 2 de la nota de aviso empresa. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Tubo endotraqueal resistencia al laser, LaserTube. Ver referencias afectadas en el anexo 2 de la nota de aviso empresa. |
| Manufacturer | WILLY RÜSCH GmbH, Alemania |
| Models | 20101, 2019-244, 19511, 102004-000040, 28022, 19451, 102004-000060, 91.822.52.89, 20081, 20021, 2019-244.LA, 20071 and 23 more |
| Event type | Safety Notice |
| Date | Jul 2, 2020 |
At a glance
- No Recall
- Yes Field safety notice
- 100–999 Matching device models in FDA data
- 100–999 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