International safety notice
Catéteres de hemodiálisis aguda de alto flujo y doble lumen MahurkarTM* 13,5 Fr (Mahurkar QPlus). Modelo: 8888135161; 8888135162; 8888135191; 8888135192; 8888135241
Spain / AEMPS · ESP · Dec 14, 2022
Key facts
| Title | Catéteres de hemodiálisis aguda de alto flujo y doble lumen MahurkarTM* 13,5 Fr (Mahurkar QPlus). Modelo: 8888135161; 8888135162; 8888135191; 8888135192; 8888135241 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Catéteres de hemodiálisis aguda de alto flujo y doble lumen MahurkarTM* 13,5 Fr (Mahurkar QPlus). Modelo: 8888135161; 8888135162; 8888135191; 8888135192; 8888135241 |
| Manufacturer | Covidien LLC, EEUU |
| Models | 1828900108, 1812900084, 20884521006376, 2113300234, 13.5FRX19.5CM, 2106900055, 8888135161, 2022-549, 1923200090, 08940, 1810000109, 1815000123 and 68 more |
| Event type | Safety Notice |
| Date | Dec 14, 2022 |
At a glance
- No Recall
- Yes Field safety notice
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