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Preguntas frecuentes
Créditos
Devices
Device Recall HIgHFlo Subcutaneous Safety Needle Sets
Modelo / Serial
Lot Numbers: 7.069/16, 7.068/16, 7.066/16, 7.065/16, 7.064/16, 7.063/16, 7.062/16, 7.061/16, 7.060/16, 7.059/16, 7.058/16, 7.057/16, 7.056/16, 7.055/16, 7.054/16, 7.053/16, 7.052/16, 7.051/16, 7.050/16, 7.049/16, 7.048/16 & 7.046/16. Expiration: 2019-02
Clasificación del producto
General Hospital and Personal Use Devices
Clase de dispositivo
2
¿Implante?
No
Distribución
Nationwide in US
Descripción del producto
HIgH-Flo Subcutaneous Safety Needle Sets, 2-Needle Set/ 24 Gauge 9mm Needles, REF/Part Numbers RMS22606, RMS22609, RMS22612, RMS12606, RMS22409, RMS32609, RMS32609, RMS12409, RMS12609, RMS62612, RMS62606, RMS12406, RMS22412, RMS12412, RMS42606, RMS62609, RMS52612, RMS42612, RMS32609, RMS22609, RMS22606, RMS42609 & RMS32612.
Manufacturer
Repro-Med Systems, Inc.
1 Event
Retiro De Equipo (Recall) de Device Recall HIgHFlo Subcutaneous Safety Needle Sets
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Fabricante
Repro-Med Systems, Inc.
Dirección del fabricante
Repro-Med Systems, Inc., 24 Carpenter Rd, Chester NY 10918-1057
Empresa matriz del fabricante (2017)
Repro-Med Systems Inc
Source
USFDA
Language
English
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