GE Healthcare has updated the Service Manuals for a number of CT and PET CT Scanners to update an incorrect torque value.
Labeling design
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 §7.55.
510(K) Database
510(K)s with Product Code = JAK and Original Applicant = GE MEDICAL SYSTEMS
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-deccaid 2 years ago
2 years agotank oil level to what level do you fill a hemit tank? Have some tilting tube spitsReply
-ACherpak 3 years ago
3 years agoDongle
ASAP!!!!
Looking for Valid dongle for GE CT. Ready to buy.
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1
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-dario1 3 years ago
3 years agoload from cold
need manual for install
brightspeed 16 slice
thanks.
Package Contents Be sure all items listed here were included with your camera. DK-25 rubber eyecup BF-1B body cap D3400 camera EN-EL14a rechargeable Li-ion AN-DC3 strap battery (with terminal cover) User’s Manual (this booklet) MH-24 battery charger (plug Warranty adapter supplied in countries or regions where required. Manual Download Agreement. These Download Terms and Conditions ('Agreement') constitute a legal agreement between you (either an individual or single entity) and Nikon Corporation or its associated company ('Nikon') setting forth the terms and conditions governing your download of the operation manual for our products (“Manual”). Nikon d3400 dslr camera user manual.
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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
Ge 16 Slice Lightspeed Manual
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
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Failure to properly document the CTDI in the Technical Reference or User Manual. Download Zmodo nvr manual download.
Class 2 Recall: GE BrightSpeed Excel/Edge/Elite Select / Elite CT..
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