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Preguntas frecuentes
Créditos
Devices
Device Recall Arterial Catheterization Kit
Modelo / Serial
Lot Numbers: (1) 13F17D0198, 13F17F0215; (2) 13F17E0029, 13F17E0537; (3) 13F17B0226, 13F17D0017, 13F17D0280; (4) 13F17A0122, 13F17C0342, 13F17E0364, 13F17E0827
Clasificación del producto
Cardiovascular Devices
Clase de dispositivo
2
¿Implante?
No
Distribución
Distributed in all 50 U.S. states and the District of Columbia. Distributed in Bahamas, Canada, Mexico, Panama, and Singapore.
Descripción del producto
(1) Arterial Catheterization Kit, Part Number (PN): ASK-04018-CC; (2) Arterial Line Kit with Sharps Safety Features, PN: ASK-04510-HUM; (3) Arterial Line Kit with Sharps Safety Features, PN: ASK-04550-UHC; (4) Arterial Catheterization Kit, PN: NA-04550-X1A
Manufacturer
Arrow International Inc
1 Event
Retiro De Equipo (Recall) de Device Recall Arterial Catheterization Kit
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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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