International safety notice
SELDICATH, MICRODARD, DISP BLOC PARA-CERVICAL DEPASST, PLEUROCATH, COMBICATH, OMBILICATH, VALVE HEIMLICH, ENDOCATH, SELDICATH, C35, C11, SELDIFLEX, V77, V78, V74
Spain / AEMPS · ESP · Jun 10, 2020
Key facts
| Title | SELDICATH, MICRODARD, DISP BLOC PARA-CERVICAL DEPASST, PLEUROCATH, COMBICATH, OMBILICATH, VALVE HEIMLICH, ENDOCATH, SELDICATH, C35, C11, SELDIFLEX, V77, V78, V74 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | SELDICATH, MICRODARD, DISP BLOC PARA-CERVICAL DEPASST, PLEUROCATH, COMBICATH, OMBILICATH, VALVE HEIMLICH, ENDOCATH, SELDICATH, C35, C11, SELDIFLEX, V77, V78, V74 |
| Manufacturer | PRODIMED, Francia |
| Models | 50037698, 50029626, 67722J23S, 50039794, 50028033, 50032325, 50029102, 50036628, 50032860, 50040785, 50037362, 50026427 and 2800 more |
| Event type | Safety Notice |
| Date | Jun 10, 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