Sarns™ Modular Perfusion System 8000 Sarns Modular Perfusion System 8000 Catalog Number Description Units/Case Base 16400 Base, 4 pump, 115V, safety monitor included 1. 134332 Sarns centrifugal cable to System 8000 1 135271 Operator's manual 1. Service manual for Sarns 9000 needed. April 11, 2011 02:10. I need a service manual for a 3M (Terumo) Sarns 9000 heart/lung machine if anyone can help. Thanks, Dean. The Terumo Sarns Modular Perfusion System 8000 is a flexible, dependable, and cost efficient modular blood pumping system.The Sarns 8000 is a modular heart-lung machine that is available in a variety of configurations. We offer 4 and 5 pumps units that are available with and without the built-in centrifugal pump.
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DESCRIPTION
The Teruno Sarns 11160 Dual Heater Cooler is a reliable, efficient patient cooling/heating system. Plant vs zombie 2 pc full.
Sarns 8000 Operating Manual
The Teruno Sarns 11160 Dual Heater Cooler is a reliable, efficient patient cooling/heating system.
FORUMSView All (5)
Ask a New Question1Reply2 years ago | 2 years agoTerumo 11160 coller/heater - Service manual Hi, i need service manual please for sarns 11160. ThanksReply |
-uams 2 years ago | 2 years agoneed a sch not cooling.need a diagram of the equipment.Reply |
2Replies3 years ago | 3 years agoTerumo 11160 Terumo 11160 service manualReply |
DOCUMENTS / MANUALSView All
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FEATURES
Sarns 8000 Service Manual
- Simple controls and high reliability
- Large capacity heater with four temperature settings
- Independent water supply and recirculating system Securecrt trial version.
SPECIFICATIONS
Height | 27.5 in |
Length | 24.5 in |
Weight | 75 lbs |
Width | 15.5 in |
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Sarns 8000 Service Manual
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Labeling mix-ups | |||||||||||||||||||||||||||
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Terumo field correction/service records were completed in 2007 and all affected units were corrected in the field in March 2007 by replacing the incorrect label at the customer location. For questions about this report call 734-741-6056. | |||||||||||||||||||||||||||
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US Nationwide Distribution - including the state of New York | |||||||||||||||||||||||||||
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 = 3M HEALTH CARE, SARNS |