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Preguntas frecuentes
Créditos
Devices
Device Recall Catheter, Intravascular, Therapeutic, ShortTerm
Modelo / Serial
Lot/Batch Numbers: 23F15L0662,23F15J0260,23F15K0983,23F15G0159,23F15J1102,23F15J0259 23F15C1225,23S15G0973,23F15H1033,23F15F0358,23F15K0345,23F15D1514 23F15C1226,23F15H0919,23F15E1091,23F15H0014,23F15D0241,23F15J0533 23F15E1094,23F15H0020,23F15H0740,23F15K1009,23F15J0431,23F15F1836 23F15H0857,23F15K0012,23F15M0313,23F15G0871,23F15J0285
Clasificación del producto
General Hospital and Personal Use Devices
Clase de dispositivo
2
¿Implante?
Yes
Distribución
US Distribution to states of: NC, OH, FL, and MD.
Descripción del producto
Catheter, Intravascular, Therapeutic, Short-Term Less than 30 days || The Arrow CVC is indicated to provide short-term (<30 days) central venous access for treatment of diseases or conditions requiring central venous access.
Manufacturer
Arrow International Inc
1 Event
Retiro De Equipo (Recall) de Device Recall Catheter, Intravascular, Therapeutic, ShortTerm
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Fabricante
Arrow International Inc
Dirección del fabricante
Arrow International Inc, 2400 Bernville Rd, Reading PA 19605-9607
Empresa matriz del fabricante (2017)
Teleflex Incorporated
Source
USFDA
Language
English
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