Model Catalog: BO-HQV 46904 (Lot serial: MFG 2015.07.31 - 2017.07.31); Model Catalog: BO-H 55815 (Lot serial: MFG 2015.07.31 - 2017.07.31); Model Catalog: CHX 30 (Lot serial: MFG 2015.07.31 - 2017.07.31); Model Catalog: BEQ-H 48730 (Lot serial: MFG 2015.07.31 - 2017.07.31); Model Catalog: BO-H 95260 (Lot serial: MFG 2015.07.31 - 2017.07.31); Model Catalog: BO-H 55161 (Lot serial: MFG 2015.07.31 - 2017.07.31); Model Catalog: BEQ-HQV 52700-1 (Lot serial: MFG 2015.07.31 - 2017.07.31); Model Catalog: BO-HQV 46901 (Lot serial: MFG 2015.07.31 - 2017.07.31); Model Catalog: BEQ-HQV 46904 (Lot serial: MFG 2015.07.31 - 2017.07.31); Model Catalog: BEQ-HQV 46900 (Lot serial: MFG 2015.07.31 - 2017.07.31); Model Catalog: BEQ-H 48761 (Lot serial: MFG 2015.07.31 - 2017.07.31); Model Catalog: BEQ-H 48721 (Lot serial: MFG 2015.07.31 - 2017.07.31); Model Catalog: BO-HQV 66606 (Lot serial: MFG 2015.07.31 - 2017.07.31); Model Catalog: BO-HQV 66605 (Lot serial: MFG 2015.07.31 - 2017.07.31); Model Catalog: BO-HQV 66604 (Lot serial
Descripción del producto
PERFUSION SET WITH SOFTLINE COATING;PLEGIOX HEAT EXCHANGER;PERFUSION TUBING PACK WITH BIOLINE COATING;CARDIOPLEGIA SET WITH SOFTLINE COATING;PERFUSION SET WITH BIOLINE COATING;CUSTOM PACK WITH SOFTLINE;CARDIOPLEGIA SET WITH BIOLINE COATING;HEART LUNG PERF
Note published by the authorities from the Netherlands: This message is a warning from the manufacturer. After placing a medical device on the market, the manufacturer is obliged to follow the device and, where necessary, to improve it. When there is a risk for the user, the manufacturer must take action. The manufacturer informs users and the inspection of this action with a warning (Field Safety Notice). See also medical device warnings. This is part of the supervision of medical technology.
Note published by the authorities from the Netherlands: This message is a warning from the manufacturer. After placing a medical device on the market, the manufacturer is obliged to follow the device and, where necessary, to improve it. When there is a risk for the user, the manufacturer must take action. The manufacturer informs users and the inspection of this action with a warning (Field Safety Notice). See also medical device warnings. This is part of the supervision of medical technology.