- Ge Lightspeed Ct Scanner User Manual 2017
- Ge Lightspeed 16 Slice Ct Scanner Specifications
- Ge Lightspeed Ct Scanner 4 Slice
Class 2 Recall: GE BrightSpeed Excel/Edge/Elite Select / Elite CT. GE has become aware of a potential set of circumstances that could cause x-ray continuation during an unexpected table stop on certain LightSpeed VCT and BrightSpeed systems. GE CT SCANNERS: GE Lightspeed Plus 4 Slice CT The GE Lightspeed Plus 4 Slice CT Scanner improves upon coverage, image quality, and exam speed when compared to models that came before it through the incorporation of vari-speed gantry rotation capability. A wide variety of ge lightspeed ct scanner options are available to you, There are 27 ge lightspeed ct scanner suppliers, mainly located in North America. The top supplying country or region is United States, which supply 48% of ge lightspeed ct scanner respectively.
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GE Healthcare - BrightSpeed Series
by GE Healthcare
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DESCRIPTION
Capable. Compact. Convenient.The BrightSpeed Series gives you full multi detector CT capabilities in three smaller systems that are as easy to select and site as they are to operate and own.
FORUMSView All (8)
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FEATURES
- Superb CT capabilities
- Powered by VCT Technology
- Ultra-compact size
- Lower life-cycle costs
SERIES MODELS
Gantry (Max. Clearance) | 70 cm |
Maximum Scan Range | 140 cm |
Slices | 8 |
Type (configuration) | Multislice |
Additional Specifications |
Gantry (Max. Clearance) | 70 cm |
Maximum Scan Range | 170 cm |
Slices | 16 |
Type (configuration) | Multislice |
Additional Specifications |
Gantry (Max. Clearance) | 70 cm |
Maximum Scan Range | 140 cm |
Slices | 16 |
Type (configuration) | Multislice |
Additional Specifications |
![Scanner Scanner](/uploads/1/3/3/2/133280420/816325719.jpg)
NEWSView All
BrightSpeed Elite with ASiR![Ge ct scanners manuals Ge ct scanners manuals](/uploads/1/3/3/2/133280420/156206004.png)
Why cant i download firefox on my mac. A new standard in CT> GE Healthcare continues its commitment to delivering high-image quality with lowered dose with the introduction of BrightSpeed Elite with ASiR (Adaptive Statistical Iterative Reconstruction). ASiR, a new technology, delivers up to 40% reduction in radiation dose along the entire body with no compromise in image quality. With .
FDA AlertsView All
Ge Lightspeed Ct Scanner User Manual 2017
Class 2 Recall BrightSpeed Excel/Edge/Elite Select Computed TomographyFailure to properly document the CTDI in the Technical Reference or User Manual. Netgear wndr3800 manual download. Download
Class 2 Recall: GE BrightSpeed Excel/Edge/Elite Select / Elite CT.Ge Lightspeed 16 Slice Ct Scanner Specifications
GE has become aware of a potential set of circumstances that could cause x-ray continuation during an unexpected table stop on certain LightSpeed VCT and BrightSpeed systems. Download https://dzyafcz.weebly.com/blog/mvk-player-for-mac.
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Ge Lightspeed Ct Scanner 4 Slice
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GE Healthcare sent an Urgent Medical Device Correction letter ' GEHC Ref# 25467-ABT or 25467' dated February 12, 2016, to all affected consignees . The letter was addressed to Hospital Administrators / Risk Managers, Managers of Radiology/Cardiology, & Radiologist/Cardiologist. The letter described the Safety Issue, Safety Instructions, Affected Product Details, Product Correction and Contact Information. Consignees were instructed to ensure that the organization that service their equipment uses the latest version of the Service Manual to maintain the safe and proper performance of their medical device. For questions call in the United States: 1-800-437-1171 or your local GE Healthcare Service Representative. For questions regarding this recall call 262-513-4122. | |||||||||||||||||||||||||||
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Worldwide Distribution - US including all states in including PR except ND, VT & WY. Foreign Distribution: ALBANIA, ARGENTINA, AUSTRALIA, AUSTRIA, BELGIUM, BOSNIA & HERZEGOVINA, BRAZIL, BULGARIA, BURKINA FASO, CAMERON, CANADA, CHILE, CHINA, COLOMBIA, DOMINICAN REPUBLIC, ESTONIA, FINLAND, FRANCE, GERMANY, GREECE, GUADELOUPE,HONG KONG, HUNGARY, ICELAND, INDIA, INDONESIA, IRA N, IRAQ, IRELAND, ISRAEL, ITALY, JAPAN, JORDAN, KENYA, REPUBLIC OF KOREA, KUWAIT, LATVIA, LEBANON, LIBYAN ARAB JAMAHIRIYA, LITHUANIA, LUXEMBOURG, MALAYSIA, MEXICO, MOROCCO, NETHERLANDS, NEW ZEALAND, NORWAY, OMAN, PERU, PHILIPPINES, POLAND, PORTUGAL, REUNION, ROMANIA, RUSSIA, SAUDI ARABIA, SINGAPORE, SLOVAKIA, SOUTH AFRICA, SPAIN, SWEDEN, SWITZERLAND, TAIWAN, TUNISIA, TURKEY, UKRAINE, UNITED ARAB EMIRATES, UNITED KINGDOM, VENEZUELA . | |||||||||||||||||||||||||||
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 ยง7.55. | |||||||||||||||||||||||||||
510(K) Database | 510(K)s with Product Code = JAK and Original Applicant = GE MEDICAL SYSTEMS |