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ced5a5f5e9 When powered by batteries, the GemStar Pump is used for ambulatory patients. FDA District: Chicago District Office. Product: Hospira GemStar Infusion System. Our focused portfolio features proven, innovative smart pump and pain management technology designed to help meet your clinical safety and workflow goals. Immediately perform proximal and distal occlusion tests as defined in the GemStar Technical Service Manual. All GemStar Infusion Pumps that were either manufactured or had a pressure sensor replaced during servicing of the pump since January 1, 2009 could be affected. For further inquiries, contact Hospira using the information provided below. The device is intended for use in intravenous, arterial, subcutaneous, short-term epidural infusion and parenteral administration of general I.V. If a device exhibits damage caused by leaking batteries, immediately remove it from clinical service and contact Hospira at 1-800-441-4100 to arrange for return of your device for repair. 5.63" h x 3.78" w x 1.93" d .
Delivery Rate Accuracy 2.5% (subject to external conditions) . Therefore, information on this site may be inappropriate for use outside of the United States. Manufacturing and Distribution Dates: February 1999 through April 2013. Pump LineSapphire . Models 13000, 13100, 13150, 13086, 13087, 13088. Product specifications below. Hospira is modifying the GemStar Technical Service Manual to add proximal and distal occlusion tests annually to confirm that devices do not require recalibration. Batteries that have exceeded their expiration date should not be used in the device, including when being used as the back-up power source along with the Power Adaptor, Docking Station, or the Battery Pack. Loss of contact can be due to a mechanical disconnect at either the positive or negative battery terminal. HTTP Error 405 - The HTTP verb used to access this page is not allowed.Internet Information Services (IIS).