PDF Yamaha Exciter Service Manual.pdf PDF Sarns 8000 Manual.pdf PDF Bentley Continental Flying Spur Workshop Manual.pdf PDF Graco King Pump Manual.pdf PDF Yamaha 140 Hp Outboard Service Manual.pdf PDF Linux Quick Reference Guide Some Useful Commands.pdf PDF Reefer Manual For A Carrier 2500a.pdf PDF Linde V1 253 Welder Manual.pdf. Sarns 8000 Roller pump for Sarns System 8000 Heart Lung Machine console, 115V, Catalog No 16402, Terumo Cardiovascular System Corp Ann Arbor, MI. The system 8000 is indicated for use in extracorporeal circulation of blood for arterial perfusion, reginal. Terumo Cardiovascular 6200 Jackson Road Ann Arbor, MI USA. Customer Service (M-F 8AM-6PM EST) Perfusion Products: 800.521.2818 CV Surgery Products: 888.758.8000.
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- Beatzit Accesories - Offering Perfusion 8000 Heart Lung Sarns Machine at Rs 2800000/unit in Thane, Maharashtra. Read about company. Get contact details and address ID: 3.
- Sarns 8000 Sarns 9000 Clinical Laboratory BECKMAN COULTER STKS BIOMERIEUX Vitek 120 Vitek 240 Vitek 30 Vitek 32 Vitek 60 Vitek Junior Vitek 2 Vital JOHNSON & JOHNSON Vitros 250 Vitros 500 Vitros 700 Vitros 700c Vitros 950.
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The Sarns Modular Perfusion System 8000 offers uncompromised reliability and safety.The Sarns Modular Perfusion System 8000 offers uncompromised reliability and
safety. Hotel front office procedures manual. Terumo’s continued engineering efforts for the Sarns System 8000 testify to its
support of perfusionists. Dedrm kindle 1.23 for mac. This trusted heart-lung machine has been used in millions
of cardiac surgery cases worldwide
safety. Hotel front office procedures manual. Terumo’s continued engineering efforts for the Sarns System 8000 testify to its
support of perfusionists. Dedrm kindle 1.23 for mac. This trusted heart-lung machine has been used in millions
of cardiac surgery cases worldwide
FORUMSView All (3)
Ask a New Question1Reply3 months ago | 3 months agoservie manuls any one have service manulsReply |
-dhanusu. N 6 years ago | 6 years agocardiology I need operating & service manual of sarns 8000 heart lung machine. . Thanks in advance Reply |
3Replies7 years ago | 7 years agoBatteries Does anyone know what batteries go in the Sarns 8000? Reply |
FEATURES
- Durable foundation - 4 or 5 pump base options
- Integrated Centrifugal System - direct connection to safety systems
- TLink Data Management System - ultimate flexibility which allows primary focus on the patient
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![Sarns 8000 service manual Sarns 8000 service manual](https://www.somatechnology.com/spanish/wp-content/uploads/2016/07/terumo_sarns_modular_perfusion_system_8000.jpg)
Sarns 8000 Service Manual
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Sarns 8000 Operating Manual
Sarns 8000 Service Manual
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The firm sent 'URGENT MEDICAL DEVICE CORRECTION' dated 11/02/2010 to customers. The letter describes the product, problem and corrective actions taken and/or needed to be taken by the customers. The letter states the system responds to a failed inductor by displaying an overspeed message and stopping the roller pump without an audible alert. The pump cannot be restarted. The customers/users are instructed to stop the pump, replace the pump with a backup or if necessary use the handcrank. The letter states that Terumo will replace the roller pump at the next preventative maintenance visit - or sooner- if the customer has a service contract. If the customer does not have a service contract, Terumo will contact the customer within 2 weeks to set up an appointment for the service. Terumo CVS expects all affected inductors to be replaced to be replaced within three months. Call Terumo CVS Customer Service upon completion of the case at 800-521-2818. The customer was also instructed to complete and return the enclosed CUSTOMER RESPONSE FORM Please note that we are not recommending that you stop using the roller pumps for your Sarns system 8000. For any questions, call toll free 800-262-3304 or phone 734-663-4145. | |||||||||||||||||||||||||||
95 roller pumps. | |||||||||||||||||||||||||||
Worldwide distribution: USA including states of CA, FL, NC and NY and countries of United Arab Emirates, China, Ecuador, and Panama. | |||||||||||||||||||||||||||
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 = JOR and Original Applicant = 3M HEALTH CARE, SARNS |