Sorin S5 Features. The S5 heart-lung-machine has a modular design. The individual components, mod- ules and accessories can be easily replaced, the overall system can be modified and extended, and the modular structure saves valuable time during routine maintenance. Koihime musou crack hongfire ag3. This established centrifugal pump system provides the S5 operator with flexibility. Service Manual, 1993 Yamaha 115 Outboard Repair Manual, Stockert S5 Operators Manual, 2016 Buick Allure Repair Manual, Sapphire Topaz Manual, Cb1000r 2015 Owners Manual, 2015toyota Corolla Maintenance Manual, 2005 Volvo S40 Haynes Repair Manual, Ford3930 Operator Manual, Study Guide For. The S5 was designed to meet the diverse needs of today's hospital—and then keep pace with you as your needs change. SIII and SIII Encore™ system users can transfer their external devices such as data management system or SCP to the new S5 System. They easily connect to the S5 using an adapter cable.
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Stockert S5 Service Manual
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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 |