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Sarns 8000 Manual

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Minitab quality companion 3 crack. Manuals can be downloaded free of charge. Paper manuals can also be purchased. Please note, Service Manuals are not available for all models. If a service manual is not available for your model, the pertinent service information has been added to the Owner's Manual. Note: If you do not have your serial number, you may use 000101 to access a.

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  • The Sarns Modular Perfusion System 8000 offers uncompromised reliability. Terumo’s continued engineering efforts for the Sarns System 8000 testify to its. Support of perfusionists. This trusted heart-lung machine has been used in millions. Of cardiac surgery cases worldwide.
  • 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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Sarns 8000 ManualThe Sarns Modular Perfusion System 8000 offers uncompromised reliability and safety.

Sarns 8000 Manual Pdf

The Sarns Modular Perfusion System 8000 offers uncompromised reliability and
safety. Blackmagic design fusion studio 9.0. Terumo’s continued engineering efforts for the Sarns System 8000 testify to its
support of perfusionists. This trusted heart-lung machine has been used in millions
of cardiac surgery cases worldwide

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-Engr.M.Saad
22 days ago		22 days agoService Manuals
I need operating & service manual of sarns 8000 heart lung machine. .Thanks in advanceReply
-Pathway Preclinical Services
6 months ago		6 months agoNeed reservoir holder
I am looking for a reservior holder for our Sarns 8000 bypass pumpReply

1

Reply
-prakash8053
a year ago		a year agoservie manuls
any one have service manulsReply

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

Sarns 8000 Manual Free

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Sarns 8000 Manual Download

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Sarns 8000 Manual

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Class 2 Device Recall Sams Modular Perfusion System 8000
Date Initiated by FirmSeptember 25, 2012
Date PostedNovember 13, 2012
Recall Status1Terminated 3 on July 11, 2013
Z-0282-2013
Recall Event ID62733
K915183
Console, heart-lung machine, cardiopulmonary bypass - Product CodeDTQ
ProductPerfusion System 8000, base 4 pump, 220V/240V safety monitor included
The Sarns' Modular Perfusion System 8000 is indicated for use for up to 6 hours on the extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures, when used by a qualified medical professional who is experienced in the operation of this or similar equipment.
Code Informationcatalog number: 16405 serial numbers: 1001-1466.
Recalling Firm/
Manufacturer		 Terumo Cardiovascular Systems Corporation
6200 Jackson Road
Ann Arbor MI 48103-9586
For Additional Information Contact
734-741-6173
Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports since 2007 of various malfunctions of the arterial and cardioplegia monitors for the Sarns Modular Perfusion System 8000. The malfunctions can be broadly categorized as follows monitor power malfunctions, inability to measure pressure and inaccurate and/or false pressure alarms. If the malfunction of the arterial or cardio
Device Design
The firm, Terumo CVS, sent an 'URGENT MEDICAL DEVICE RECALL' notice/Safety Advisory Alert dated September 24, 2012 and an addendum to the Operator's Manual to alert all affected Customers. The notice described the product, problem and actions to be taken. The customers were instructed to review this medical device recall notice; assure that all users are aware to this notice; place the addendum in the Operator's Manual just before page 4.1 and complete and return the attached Customer Response Form via Fax to: 1-734-741-6149 or email to:www.termuo-cvs.com. If you have any questions or concerns contact Terumo CVS Customer Service at 1-800-521-1818; Monday - Friday, 8 AM - 6 PM ET.
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Worldwide distribution: USA (nationwide) including states of: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NH, NJ, NM, NY, OH, OK, OR, PA, RI, SC, TN, TX, VA, WA, WI, WV, and WY; and countries of: ARGENTINA, AUSTRALIA, BANGLADESH, BRAZIL, CALI COLOMBIA, CALLO PERU, GERMANY, GUAYQUIL ECUADOR, HONG KONG, INDIA, INDONESIA, JAPAN, LEBANON, MADRID SPAIN, MEXICO, NEW ZEALAND, SANTIAGO, SANTIAGO CHILE, SINGAPORE, SOUTH AFRICA, SOUTH KOREA, SRI LANKA, TAIWAN, THAILAND, and UNITED ARAB EMIRATES (UAE).
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) Database510(K)s with Product Code = DTQ and Original Applicant = 3M HEALTH CARE, SARNS