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Preguntas frecuentes
Créditos
Devices
Device Recall Deltec PortACath
Modelo / Serial
Lot M27037
Distribución
The recalled products were shipped nationwide in the United States and worldwide.
Descripción del producto
Port-A-Cath II Epidural Low Profile Polysulfone/Titanium Access System, with PolyFlow Polyurethane Catheter, 1.2mm O.D. x 5mm I.D., REF 21-1501-22
Manufacturer
Deltec, Inc
1 Event
Retiro De Equipo (Recall) de Device Recall Deltec PortACath
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Fabricante
Deltec, Inc
Dirección del fabricante
Deltec, Inc, 1265 Grey Fox Rd, Saint Paul MN 55112-6929
Source
USFDA
18 dispositivos con un nombre similar
Más información acerca de la data
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Device Recall Deltec PortACath
Modelo / Serial
Lot M27052
Clasificación del producto
General Hospital and Personal Use Devices
Clase de dispositivo
3
¿Implante?
No
Distribución
The recalled products were shipped nationwide in the United States and worldwide.
Descripción del producto
Port-A-Cath II Low Profile Epidural Implantable Access System, with PolyFlow Polyurethane Catheter, 1.2mm O.D. x 0.5mm I.D., REF 21-1501-01
Manufacturer
Deltec, Inc
Device Recall Deltec PortACath
Modelo / Serial
Lot M27134
Clasificación del producto
General Hospital and Personal Use Devices
Clase de dispositivo
2
¿Implante?
Yes
Distribución
The recalled products were shipped nationwide in the United States and worldwide.
Descripción del producto
Port-A-Cath Titanium Venous Access System, with Silicone Catheter, 2.8mm O.D. x 1.0mm I.D., 9 Fr Introducer Set, REF 21-4009-24
Manufacturer
Deltec, Inc
Device Recall Deltec PortACath
Modelo / Serial
Lot M27051
Clasificación del producto
General Hospital and Personal Use Devices
Clase de dispositivo
2
¿Implante?
Yes
Distribución
The recalled products were shipped nationwide in the United States and worldwide.
Descripción del producto
Port-A-Cath Low Profile Titanium Venous Access System, with Silicone Catheter, 2.8mm O.D. x 1.0mm I.D., 9 Fr Introducer Set, REF 21-4035-24
Manufacturer
Deltec, Inc
Device Recall Deltec PortACath
Modelo / Serial
Lots M27118 and M27262
Clasificación del producto
General Hospital and Personal Use Devices
Clase de dispositivo
2
¿Implante?
Yes
Distribución
The recalled products were shipped nationwide in the United States and worldwide.
Descripción del producto
Port-A-Cath Low Profile Titanium Venous Access System, with PolyFlow Polyurethane Catheter, 1.9mm O.D. x 1.0mm I.D., 6 Fr Introducer Set, REF 21-4037-24
Manufacturer
Deltec, Inc
Device Recall Deltec PortACath
Modelo / Serial
Lot M26890
Clasificación del producto
Cardiovascular Devices
Clase de dispositivo
2
¿Implante?
No
Distribución
The recalled products were shipped nationwide in the United States and worldwide.
Descripción del producto
6 Fr Introducer Set, REF 21-2320-24
Manufacturer
Deltec, Inc
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