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Devices
Fresenius LIBERTY 05087212 Automated Peritoneal Dialysis System Line Cycler Set
Modelo / Serial
Lot Number Expiration Date 09AR08026 1/31/2012 09AR08045 1/31/2012 09AR08046 . 11/30/2011 09AR08092 1/31/2012 09AR08093 1/31/2012 09AR08103 1/31/2012 09AR08104 01/31/2012 09AR08119 11/30/2011 09BR08034 02/29/2012 09BR08035 2/29/2012 09BR08036 02/29/2012 09BR08037 2/29/2012 09BR08038 02/29/2012 09BR08050 2/29/2012 09BR08051 02129/2012 09BR08052 02129/2012 09BR08073 02129/2012 09BR08074 2/29/2012 09BR08801 02/29/2012 09BR08802 02/29/2012 09BR08803 2/29/2012 09CR08018 3/31/2012 09CR08019 3/31/2012 09CR08032 3/31/2012 09CR08033 03/31/2012 09CR08034 3/31/2012 09CR08035 3/31/2012 09CR08095 3/31/2012 09DR08001 4/30/2012 09DR08002 04/30/2012 09DR08023 4/30/2012 09DR08037 4/30/2012 09DR08039 4/30/2012 09DR08040 04130/2012 09ER08093 05131/2012 09ER08094 05131/2012 09ER08095 05131/2012 09ER08096 05131/2012 09ER08097 5/31/2012 09ER08104 05/31/2012 09HR08072 06/30/2012 09HR08073 6/30/2012 09HR08074 06/30/2012 09HR08099 06/30/2012 09HR08100 06/30/2012 09HR08101 6/30/2012 09HR08130 06/30/2012 09HR08131 06/30/2012 09JR08016 07/31/2012 09JR08017 07/31/2012 09JR08018 07/31/2012 09JR08019 7/31/2012 09JR08095 07131/2012 09JR08096 07131/2012 09JR08097 713112012 09JR08106 713112012 09KR08007 813112012
Clasificación del producto
Gastroenterology-Urology Devices
Clase de dispositivo
2
¿Implante?
No
Distribución
Nationwide Distribution: Throughout USA.
Descripción del producto
LIBERTY Automated Peritoneal Dialysis System Line Cycler Set with stay safe connectors (Dual Patient Connector) PIN: 050-87212, manufactured for Fresenius Medical Care, Waltham MA by Erika de Reynoza, Reynosa Tampa, Mexico.
Manufacturer
Fresenius Medical Care Holdings, Inc.
1 Event
Retiro De Equipo (Recall) de Fresenius LIBERTY 05087212 Automated Peritoneal Dialysis System Line Cycler Set
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Fabricante
Fresenius Medical Care Holdings, Inc.
Dirección del fabricante
Fresenius Medical Care Holdings, Inc., 920 Winter St, Waltham MA 02451-1521
Empresa matriz del fabricante (2017)
Fresenius SE & Co KGaA
Source
USFDA
Language
English
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