Windows is in notification period. The perfusion record is a legal record of the cardiopulmonary bypass (CPB) procedure and should be an accurate and legible document. Traditionally, the perfusion record has been handwritten, with the perfusionist documenting specific parameters and events, often every 5–10 minutes or when changes in monitored parameters occur or events dictate documentation (e.g., drug administration). Aims of the manual This manual is intended to provide specialized information about programming the CPU 928B for users who already have basic knowledge of programming PLCs and want to use the CPU 928B in the S5-135U programmable controller. Vegas pro full version. If you do not yet have this basic knowledge, we strongly advise you read the documentation.
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Stockert S5 Gas Blender Manual
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Stockert S5 Manual Download
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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. | |||||||||||||||||||||||||||
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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 |