International safety notice
PNEUMOCATH®/NEO-PNEUMOCATH®/THORACATH® Ver referencias afectadas en el anexo I de la nota de aviso de la empresa
Spain / AEMPS · ESP · Sep 15, 2020
Key facts
| Title | PNEUMOCATH®/NEO-PNEUMOCATH®/THORACATH® Ver referencias afectadas en el anexo I de la nota de aviso de la empresa |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | PNEUMOCATH®/NEO-PNEUMOCATH®/THORACATH® Ver referencias afectadas en el anexo I de la nota de aviso de la empresa |
| Manufacturer | intra special catheters GMBH. Alemania |
| Models | 04025562506124, 04025562505011, 2020-526, 01.09.2020, 04025562500122, 28022, 04025562507114, 04025562500115, 90001, 04025562504014, 61954, 46026 and 23 more |
| Event type | Safety Notice |
| Date | Sep 15, 2020 |
At a glance
- No Recall
- Yes Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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