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Preguntas frecuentes
Créditos
Devices
Device Recall POWERPORT(R) ClearVUE(R) Slim with Smooth Septum, 8F Polyurethane Catheter with Open Suture Holes
Modelo / Serial
Lot Number Unique Device Identifier (UDI) REAN0067 (01)00801741110825(17)170628(10)REAN0067 REAP0630 (01)00801741110825(17)170728(10)REAP0630 REAS2309 (01)00801741110825(17)171028(10)REAS2309 REAV2088 (01)00801741110825(17)171028(10)REAV2088 REAY0330 (01)00801741110825(17)171031(10)REAY0330 REBS1275 (01)00801741110825(17)180731(10)REBS1275 REBT1568 (01)00801741110825(17)181031(10)REBT1568 REBV0713 (01)00801741110825(17)181231(10)REBV0713
Clasificación del producto
General Hospital and Personal Use Devices
Clase de dispositivo
2
¿Implante?
Yes
Distribución
Nationwide
Descripción del producto
POWERPORT ClearVUE Slim with Smooth Septum, 8F ChronoFlex, Polyurethane Catheter with Open Suture Holes, REF 1678301
Manufacturer
Bard Peripheral Vascular Inc
1 Event
Retiro De Equipo (Recall) de Device Recall POWERPORT(R) ClearVUE(R) Slim with Smooth Septum, 8F Polyurethane Catheter with Open Suture Holes
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Fabricante
Bard Peripheral Vascular Inc
Dirección del fabricante
Bard Peripheral Vascular Inc, 1625 W 3rd St Bldg 1, Tempe AZ 85281-2438
Empresa matriz del fabricante (2017)
Becton, Dickinson and Company
Source
USFDA
Language
English
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