International safety notice
Catéter de oclusión aórtico LeMaitre, nº de referencia 2107-80 y 2107-81
Spain / AEMPS · ESP · Jun 3, 2021
Key facts
| Title | Catéter de oclusión aórtico LeMaitre, nº de referencia 2107-80 y 2107-81 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Catéter de oclusión aórtico LeMaitre, nº de referencia 2107-80 y 2107-81 |
| Manufacturer | LeMaitre Vascular, Inc. Alemania |
| Models | OLC1059, 28023, OLC1057, OLC1047, OLC1061, OLC1039, 01803, OLC1048, OLC1041, OLC1050, OLC1037, OLC1068 and 34 more |
| Event type | Safety Notice |
| Date | Jun 3, 2021 |
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