International safety notice
Kit de plasmaféresis (PEX) para el equipo AMPLYA Acute Multitherapeutic System™. Nº de Catálogo IB0590040.
Spain / AEMPS · ESP · Oct 23, 2018
Key facts
| Title | Kit de plasmaféresis (PEX) para el equipo AMPLYA Acute Multitherapeutic System™. Nº de Catálogo IB0590040. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Kit de plasmaféresis (PEX) para el equipo AMPLYA Acute Multitherapeutic System™. Nº de Catálogo IB0590040. |
| Manufacturer | BELLCO S.r.l., Italia. |
| Models | KABLP05, 1807000241, IB0590040, 48312, LOTE1807000241, 75-77, 08172, FA847, 2018-546 |
| Event type | Safety Notice |
| Date | Oct 23, 2018 |
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