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- LivaNova Sorin Stockert S5 Features. Formerly referred to as the Sorin S5 or Stockert S5, the LivaNova S5 heart-lung machine is the 5th generation perfusion system that offers great functionality, flexibility, and quality. The S5 perfusion device allows for better integration with the perfusion circuit, more configuration options to accommodate more procedures including pediatric.
- The S5 control panel MRP 150/85 differs from the S5. Control panel MRP 85 in that the S5 control panel MRP 150/ 85 is used to control a mast-roller pump 150 or 85 and the. S5 control panel MRP 85 is used to control two MRP 85. S5 mast roller pump 150/85 (abbreviation: mast pump) 1.6. Mast-mounted roller pumps consist of a pump unit (pump.
- Extracorporeal circulation at work with my control. This pump is STOCKERT S5 and another device is VAVD.
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Minimum system requirements are: - Adobe Acrobat 9, Adobe Acrobat 10, Adobe Acrobat DC - Internet Explorer, Google Chrome, Mozilla Firefox, Safari. 6.8 Manual ventilation During manual ventilation of the patient, the switch of the APL valve is set to the MAN position. One piece all episode subtitle indonesia mp4. Only the warnings/alarms for the lower O2 alarm, for the upper airway pres-sure (Paw) and for CO2 are enabled. The piston of the VGC is in the upper end position in order to reduce the dead space volume of the ventilator.
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The firm, Sorin Group, sent an 'URGENT FIELD SAFETY NOTICE' dated September 19, 2012 to all affected customers by certified mail. The notice described the product, problem and actions to be taken. The customers were instructed to follow the provided instructions for the continued safe use of the Perfusion systems until they have been serviced or replaced by Sorin Group. The Sorin Group Service Team will contact the customer to schedule servicing and replacement of the affected product. The customers were also instructed to complete and return the Customer Response Form via fax to 303-467-6502 or by email to [email protected]; assure this notice is distributed to all personnel who need to be aware of this notice; and if they have transferred the affected products to a third party, pass this information with them as well as with Sorin Group Customer Service at 1-800-650-2623. For questions regarding this notice, contact Sorin Group USA Customer Service at 1-800-650-2623. | |||||||||||||||||||||||||||
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Worldwide distribution: USA (nationwide) including states of: AZ, GA, MI, MS, NC, NY, PA, SC, and TX; and countries of: Austria, Australia, Belgium, Canada, People's Republic of China, Columbia, Denmark, Finland, Germany, India, Iran-Islamic Republic of, Ireland, Japan, Lebanon, Morocco, Pakistan, Poland, Russian Federation, Saudia Arabia, Spain, South Africa, Thailand, Turkey and United Kingdom. | |||||||||||||||||||||||||||
TPLC Device Report | |||||||||||||||||||||||||||
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls. 2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall. 3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55. | |||||||||||||||||||||||||||
510(K) Database | 510(K)s with Product Code = DTQ and Original Applicant = SORIN GROUP DEUTSCHLAND GMBH |