Toshiba Artida Ultrasound User Manual

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• Description Toshiba Aplio Artida. In keeping with Toshiba’s commitment to delivering quality ultrasound equipment, the Toshiba Aplio Artida is a stand-alone ultrasound system that provides exceptional images, superior performance, streamlines workflow and increases productivity all while being highly personalized with advanced imaging capabilities.
• View and Download Toshiba Aplio 500 TUS-A500 operation manual online. DIAGNOSTIC ULTRASOUND SYSTEM. Aplio 500 TUS-A500 medical equipment pdf manual download.

FEATURES
Scanning method
• Electronic Convex
• Electronic Linear
• Endovaginal
Display modes
• B Mode (Single, Dual)
• M Mode
• B/M Mode
B-Mode
• Depth of field: 20cm maximum
• Display shift: Vertical, Left/Right, Top/Bottom reversal
M-Mode
• Display method: Moving Bar Display
• Sweep speeds: Four selections
Operating functions
• Modality specific 8-selection image processing
• Auto-focus

Toshiba Partida Ultrasound User Manuals

• Real-time four-step zoom
User interface
• 9' high-resolution monitor (12' monitor optional)
• Adjustable tilt-swivel monitor
• Height-adjustable control console
• Alpha-numeric keyboard
Power source
• 100, 110, 115, 117, 127, 220, 230, 240
• VAC +/-10%
• 50/60 Hz, 500VA, 120 VA (main unit)
DIMENSIONS
18'W x 25'D x 45'-50'H

TRANSDUCERS

• PVG-366M 3.75 MHz Convex
• PVG-720S 7.5 MHz Convex
• PVG-601V 6.0 MHz Endovaginal
• PVG-381M 3.75 MHz Tightly-Curved Convex
• P~T-738F 7.0 MHz Micro-probe
• PVF-738l1 7.0 MHz Micro-probe
• PVF-745V 7.0 MHz Micro-probe

Toshiba Partida Ultrasound User Manual Instructions

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Toshiba Partida Ultrasound User Manual User

Toshiba Partida Ultrasound User Manual Pdf

New Search Back to Search Results Class 2 Device Recall SSH880CV Aplio Artida; System, Diagnostic Ultrasound Date Initiated by Firm September 28, 2010 Date Posted March 03, 2011 Recall Status1 Terminated 3 on May 02, 2012 Z-1498-2011 Recall Event ID 57303 K090158 System, imaging, pulsed echo, ultrasonic - Product CodeIYO Product SSH-880CV Aplio Artida; System, Diagnostic Ultrasound Code Information Serial Numbers (last 4): 2031, 2033, 2069, 2070, 2072, 2073, 2074, 2076, 2077, 2079, 2087, 2088, 2103, 2105, 2107, 2120, 2205, 2206, 2218, 2219, 2220, 2260, 2262, 2268, 2270, 2271, 2272, 2273, 2280, 2281, 2311, 2313, 2334, 2335, 2340, 2341, 2347, 2348, 2360, 2361, 2389, 2390, 2405, 2032, 2048, 2049, 2056, 2071, 2075, 2078, 2080, 2104, 2106, 2108, 2119, 2123, 2124, 2204, 2261, 2282, 2296, 2297, 2312, 2342, 2389, 2390, 2405 Recalling Firm/ Manufacturer Toshiba American Medical Systems Inc 2441 Michelle Dr P.O. Box 2068 Tustin CA 92781-2068 For Additional Information Contact 714-730-5000 Toshiba America Medical Systems is initiating a field correction on the SSH-880CV Aplio Artida Diagnostic Ultrasound System due to software issues. Software design Toshiba America Medical Systems (TAMS) sent an URGENT MEDICAL DEVICE CORRECTION letter to consignees via USPS return receipt mail. The letter contained a return reply form that is to be faxed to TAMS at 877-349-3054 as proof of notification. Customers were instructed to share the information with all users and reviewing radiologists as well as clinical engineering or biomedical group at their facility. For questions regarding this recall call 800-421-1968 or 800-521-1968. 40 units Nationwide Distribution to CA, GA, IA, IL KY, LA, MA, MN, MT, OH, OR, PA, TX, WI, and Puerto Rico. 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 = IYO and Original Applicant = TOSHIBA AMERICA MEDICAL SYSTEMS, INC.