Philips Epiq 5 User Manual Pdf

Posted : admin On 10/6/2021
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DESCRIPTION
EPIQ 5 features our most powerful architecture ever applied to ultrasound imaging.

EPIQ 5 & 7 Training Manual Module 1 Introduction This manual is specific to the OEM Philips models EPIQ 5 and EPIQ 7 field service training presented by the Conquest Imaging training department. After completing the training, you will: Understand overall system operation. EPIQ Series Service Manual - Free ebook download as PDF File (.pdf), Text File (.txt) or view presentation slides online. This document must be returned to Philips when the user is no longer licensed and in any event upon Philips first written request. Table 14-5 EPIQ 5 System Enclosures. This section covers system frontend topics for the EPIQ 5 and EPIQ 7. Front end is a general term for the parts of the ultrasound system that receive the reflections from acoustic energy that have been transmitted into the body and perform the various signal processing functions needed to produce an ultrasound image. The following are. EPIQ 5 is supported by Philips leading-edge Anatomical Intelligence. Improved clinical information from each scan, faster and more consistent exams that are easier to perform, and a higher level of confidence, even for technically difficult patients. Offering a complete set of easy-to-use quantitative tools. ManufacturedbyPhilipsUltrasound 22100Bothell-EverettHighway Bothell,WA USA Telephone:+1425-487-7000or800-426-2670 Fax:+1425-485-6080 www.healthcare.philips.

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-Timmyhaines14
6 months ago
6 months agoError code 031
Hello, has anyone encountered error code 031 transducer reselect? Reply
-ice
3 years ago
3 years ago508 error
hi has any one seen this error on a Philips epiq 5g.i was wondering if somebody has an architectural diagram maybe for this machine so i might pinpoint the cause ? Reply

1

Reply
-NHA_Chad
3 years ago
3 years agoDICOM Selection - grey'd out
I need to set my DICOM SR server as active in the DICOM selection menu however it is grey'd out and I figure out how to get in there. Any ideas?Thank you,Reply

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FEATURES

  • The new challenges in global healthcare
  • Unprecedented advances in premium ultrasound performance can help address the strains on overburdened hospitals and healthcare systems, which are continually being challenged to provide a higher quality of care cost-effectively. The goal is quick and accurate diagnosis the first time and in less time. Premium ultrasound today demands improved clinical information from each scan, faster and more consistent exams that are easier to perform, and a higher level of confidence, even for technically difficult patients.
  • More confidence in the diagnoses even for the most difficult cases
  • Proprietary nSIGHT Imaging architecture introduces a totally new approach to forming ultrasound images without compromise. nSIGHT Imaging strengthens the power of PureWave, useful in imaging technically difficult patients.
  • EPIQ 5 offers a wide variety of sophisticated Q-Apps to quantify ultrasound image information. It’s the most intelligent premium ultrasound system ever, offering a complete set of easy-to-use quantitative tools.
  • Anatomical Intelligence is the heart of EPIQ 5
  • Philips exclusive Anatomical Intelligence Ultrasound (AIUS) is designed to elevate the ultrasound system from a passive to an actively adaptive device. With advanced organ modeling, image slicing, and proven quantification, exams are easy to perform, more reproducible, and deliver new levels of clinical information.
  • Designed to reinvent the user experience
  • EPIQ 5 has completely reinvented the premium ultrasound user experience. Ease of use, workflow, ergonomics, portability and they've revolutionized how the user interacts with an ultrasound system from every standpoint, and kept it beautifully intuitive and very quiet.
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Philips Epiq 7 Specifications

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Class 2 Device Recall EPIQ 5 Ultrasound System, Model: EPIQ 5G, EPIQ 5C, EPIQ 5W
Date Initiated by FirmNovember 05, 2014
Date PostedDecember 16, 2014
Recall Status1Terminated 3 on August 15, 2016
Z-0816-2015
Recall Event ID69790
K132304
System, imaging, pulsed doppler, ultrasonic - Product CodeIYN
ProductEPIQ 5 Ultrasound System, EPIQ 5 systems with software versions 1.0.x or 1.1.x with QLAB a2DQ and/or aCMQ plug-ins are affected. Model: EPIQ 5G, EPIQ 5C, EPIQ 5W. Catalog Number: 795204 / 795205 and Part Number: 989605408541
Diagnostic Ultrasound Imaging.
Code InformationSERIAL NUMBERS FOR FCO 79500317-EPIQ5 system: US114B0005, US114B0006, US114C0193, US114C0209, US114C0239, US114C0240, US114C0241, US114C0271, US114C0272, US114C0273, US114C0284, US114C0286, US114C0287, US114C0308, US114C0331, US114C0334, US114C0366, US114C0751, US214C0043, US214C0106, US214C0140, US214C0143, US214C0144, US214C0416, US214C0417, US314C0199, US314C0298, US314C0447, US314C0728, US314C0745, US314C0800, US314C0801, US414C0012, US414C0066, US414C0114, US414C0157, US414C0158, US414C0159, US414C0395, US514C0081, USD13B0662, USD13C0033, USD13C0234, USD13C0290, USD13C0291, USD13C0481, USD13C0525, USD13C0526, USD13C0527, USD13C0572, USD13C0573, USD13C0584, USD13C0709, USN13B0039, USN13C0018, USN13C0182, USN13C0183, USN13C0184, USN13C0186, USN13C0206, USN13C0281, USN13C0282, USN13C0283, USN13C0284, USN13C0285, USN13C0286, USN13C0312, USN13C0361, USN13C0502, USN13C0503, USN13C0580, USN13C0654, USO13C0352, USO13C0354, USO13C0355, USO13C0356, USO13C0368, USO13C0369, USO13C0395, USO13C0396, USO13C0397, USO13C0398, USO13C0405, USO13C0453, USO13C0454, USO13C0596, USO13C0678, and USO13C0685.
Recalling Firm/
Manufacturer
Philips Ultrasound, Inc.
22100 Bothell Everett Hwy
Bothell WA 98021-8431
For Additional Information ContactCustomer Service
425-482-8466
When using the QLAB Auto 2D Quantification (a2DQ) and Auto Cardiac Motion Quantification (aCMQ) applications, the reported End-Systolic Volume (ESV) may be smaller, and the Left Ventricular Ejection Fraction (EF) may be higher, than the ESV and EF calculated by manual tracing without the use of QLAB. An incorrect EF calculation could lead to misdiagnosis and/or delayed or incorrect therapy.
Software design
Philips has identified additional affected units and sent the Urgent-Field Safety Notice -Philips Ultrasound QLAB 10.0 (on Xcelera) letter, dated 2015/3/17, to their consignees. The FCO associated with this letter is FSN MA-FCO 83000190. The affected units identified as QLAB versions 10.0 with a2DQ and/or aCMQ plug-ins installed with Philips Xcelera software. QLAB software installed on Philips diagnostic ultrasound systems (carts) is the subject of a separate Field Safety Notice (FSN MA-FCO79500316 ). Philips has corrected this issue with QLAB version 10.2 on Xcelera and will contact customers to arrange installation of the upgrade to version 10.2 or higher free of charge. If consignees need any further information or support concerning the FCO 83000190, please contact your local Philips representative or Philips Customer Service at 1-800-722-9377. *************************************************************************************** Philips has begun sending out the URGENT - Medical Device Correction letters, dated 2014 NOV 05, for the Philips Ultrasound QLAB, Philips Model EPIQ 5 Ultrasound System, Philips Model EPIQ 7 Ultrasound System, and Philips Ultrasound Q-Station. The customer letter is also identified with the FSN # 79500316; 79500317; 79500318; or 79500321. The letters notified customers that Erroneous End-Systolic Volumes and Ejection Fraction May Be Reported When Using a2DQ & aCMQ (Auto 2D Quantification & Auto Cardiac Motion Quantification). Customers with questions should contact local Philips representative or Philips Customer Service at 1-866-767-7822.
88 units (42 in the US and 46 outside US)
Worldwide distribution (for FCO 83000190): US, including the states of AK, CA, CO, CT, DC, DE, FL, GA, ID, IL, IN, KS, KY, MA, MD, ME, MI, MN, MO, NC, NJ, NY, OH, OR, PA, SC, SD, TN, TX, VA, WA, and WI; and the countries of United Arab Emirates, Austria, Australia, Belgium, Canada, Switzerland, Colombia, Germany, Ecuador, Estonia, Spain, Finland, France, Great Britain, Hong Kong, Israel, Italy, Japan, Luxembourg, Malaysia, Netherlands, Norway, New Zealand, Philippines, Saudi Arabia, Sweden, Singapore, Slovenia, Thailand, Turkey, Taiwan, and Vietnam. ********************************************************************************** Worldwide Distribution -- US, including the states of KY, TN, ME, CA, PA, NC, CT, NY, SC, IL, IN, and WI; and the countries of Argentina, Spain, India, Italy, Austria, Germany, Belgium, Canada, Finland, Switzerland, Greece, Malaysia, Sweden, Australia, Netherlands, Mexico, Peru, Taiwan, Japan, France, and Norway.
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 = IYN and Original Applicant = PHILIPS ULTRASOUND, INC.