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System, X-Ray, Stationary

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Description
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Advanced Universal U-Arm Stand 4000
KONICA MINOLTA MEDICAL IMAGING U.S.A., INC.
Advanced Universal U-arm Stand 4000 - Motorized Auto Positioning and Touchscreen control
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Advanced Universal U-Arm Stand 3000
KONICA MINOLTA MEDICAL IMAGING U.S.A., INC.
Advanced Universal U-arm Stand 3000 - 8' Motorized Auto Positioning and Touchscreen control
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U-Arm System
KONICA MINOLTA MEDICAL IMAGING U.S.A., INC.
Universal U-arm system - With Motorized Auto Positioning and Touchscreen control
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U-Arm System Basic
KONICA MINOLTA MEDICAL IMAGING U.S.A., INC.
Universal U-arm system - Motorized.
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Straight Arm System
KONICA MINOLTA MEDICAL IMAGING U.S.A., INC.
Universal Radiographic Straight Arm system variable focal distance left loading Only.
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Radmedix AcuityUDR
RADMEDIX, LLC
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Radmedix AcuitySDR+
RADMEDIX, LLC
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Radmedix AcuitySDR
RADMEDIX, LLC
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Radmedix AcuityCDR
RADMEDIX, LLC
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Radmedix AcuityFDR+
RADMEDIX, LLC
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Radmedix AcuityFDR
RADMEDIX, LLC
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AcuitySDR
RADMEDIX, LLC
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AcuitySDR
RADMEDIX, LLC
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Radmedix
RADMEDIX, LLC
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Radmedix
RADMEDIX, LLC
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Radmedix
RADMEDIX, LLC
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Radmedix
RADMEDIX, LLC
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Radmedix
RADMEDIX, LLC
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AcuitySDR
RADMEDIX, LLC
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AcuitySDR
RADMEDIX, LLC
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AcuitySDR
RADMEDIX, LLC
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AcuitySDR
RADMEDIX, LLC
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AcuitySDR
RADMEDIX, LLC
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AcuitySDR
RADMEDIX, LLC
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uDR
UIH TECHNOLOGIES LLC
The uDR 780i digital medical x-ray system is intended for use by a qualified/trained doctor or technician on both adult and pediatric subjects for taking diagnostic radiographic exposures of the skull, spinal column, chest, abdomen, extremities, and other anatomic sites. Applications can be performed with the subject sitting, standing, or lying in the prone or supine position. Not for mammography.
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uDR
UIH TECHNOLOGIES LLC
The uDR 596i Radiographic system is intended to be used by a qualified/trained doctor or technician on both adult and pediatric subjects for taking diagnostic radiographic exposures of the skull, spinal column, chest, abdomen, extremities, limbs and trunk. Not for mammography.
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Halifax Imaging Kit
Halifax Biomedical Incorporated
The Halifax Imaging Kit is part of the SR Suite product line, provides an alternative path tocreating an SR Suite. The Halifax Imaging Kit is comprised of FDA cleared or certified X-Raycomponents integrated into an existing digital radiography room already containing an FDAcleared x-ray imaging system to form an SR Suite. The exposures of the Halifax Imaging Kitand the existing DR system are synchronized by replacing the trigger switches of the twosystems with the Halifax Synchronization Switch. The Halifax Synchronization Switchensures the two X-Ray imaging systems fire simultaneously, providing a pair of X-Ray imagesfrom two different perspectives to be taken at the exact same time. This process allows forRoentgen Stereophotogrammetric Analysis (RSA) or stereo orthopaedic radiography (SOR).RSA is a stereo x-ray technique that enables measurements more accurate and precise thansingle plane radiography based on phantom studies. The increased level of precision enablesmeasurement of implant stability.
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Definium
Hangwei GE Medical Systems Co., Ltd.
Definium Tempo System UDI
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Definium
Hangwei GE Medical Systems Co., Ltd.
Definium Tempo Pro System UDI
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DRX-Compass X-ray System
CARESTREAM HEALTH, INC.
XRAY OTC 80KW 400KHU AUTOTILT CF OSHPD
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PodSKAN HF Diagnostic X-ray System
SKANRAY TECHNOLOGIES LIMITED
PodSKAN is an advanced high frequency type X-Ray system designed for superior image quality with powerful 2.8KW generator and very low leakage radiation. The system houses two microprocessors, one for control/supervisory functions and another one man-machine/User interface. It can be easily plugged into 16A Wall socket with 120 VAC or 240 VAC, 50/60 Hz.. The technology incorporates feedback circuits to ensure highest accuracy & reproducibility of X-Ray output.
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ExamVue
JPI HEALTHCARE. CO., LTD.
ExamVue Duo is a software program designed to provide image acquisition, processing and operational management functions for digital radiography and use by radiologists and radiology technicians. ExamVue Duo saves the digital X-ray images acquired from the detector and process it to make the better image quality. The software also manages patient information, capture, and store diagnostic images in an internal database. It also supports DICOM 3.0 protocol which allows compatibility with the network programs such as the PACS system.
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Samsung Electronics Co., Ltd.
The GF85 Digital X-ray Imaging System is intended for use in generating radiographic images of human anatomy by a qualified/trained doctor or technician. This device is not intended for mammographic applications.
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Samsung Electronics Co., Ltd.
The GF85 Digital X-ray Imaging System is intended for use in generating radiographic images of human anatomy by a qualified/trained doctor or technician. This device is not intended for mammographic applications.
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GXR-ES,ECS Diagnostic X-ray System
DRGEM Corporation
The DRGME’s directive DR-QP-0708-03_DI code assignment specifies that the UDI (Unique Device Identifier) is assigned based on the system model name, power specifications, and maximum x-ray tube voltage of the x-ray tube. *Power Specification (V) / maximum tube Voltage (kV) : 100-120 V~ / 125kV
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GXR-ES,ECS Diagnostic X-ray System
DRGEM Corporation
The DRGME’s directive DR-QP-0708-03_DI code assignment specifies that the UDI (Unique Device Identifier) is assigned based on the system model name, power specifications, and maximum x-ray tube voltage of the x-ray tube. *Power Specification (V) / maximum tube Voltage (kV) : 100-120 V~ / 125kV
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GXR-ES,ECS Diagnostic X-ray System
DRGEM Corporation
The DRGME’s directive DR-QP-0708-03_DI code assignment specifies that the UDI (Unique Device Identifier) is assigned based on the system model name, power specifications, and maximum x-ray tube voltage of the x-ray tube. *Power Specification (V) / maximum tube Voltage (kV) : 100-120 V~ / 125kV
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GXR-ES,ECS Diagnostic X-ray System
DRGEM Corporation
The DRGME’s directive DR-QP-0708-03_DI code assignment specifies that the UDI (Unique Device Identifier) is assigned based on the system model name, power specifications, and maximum x-ray tube voltage of the x-ray tube. *Power Specification (V) / maximum tube Voltage (kV) : 100-120 V~ / 125kV
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GXR-ES,ECS Diagnostic X-ray System
DRGEM Corporation
The DRGME’s directive DR-QP-0708-03_DI code assignment specifies that the UDI (Unique Device Identifier) is assigned based on the system model name, power specifications, and maximum x-ray tube voltage of the x-ray tube. *Power Specification (V) / maximum tube Voltage (kV) : 100-120 V~ / 125kV
0
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GXR-ES,ECS Diagnostic X-ray System
DRGEM Corporation
The DRGME’s directive DR-QP-0708-03_DI code assignment specifies that the UDI (Unique Device Identifier) is assigned based on the system model name, power specifications, and maximum x-ray tube voltage of the x-ray tube. *Power Specification (V) / maximum tube Voltage (kV) : 200-240 V~ / 125kV
0
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GXR-ES,ECS Diagnostic X-ray System
DRGEM Corporation
The DRGME’s directive DR-QP-0708-03_DI code assignment specifies that the UDI (Unique Device Identifier) is assigned based on the system model name, power specifications, and maximum x-ray tube voltage of the x-ray tube. *Power Specification (V) / maximum tube Voltage (kV) : 200-240 V~ / 125kV
0
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GXR-ES,ECS Diagnostic X-ray System
DRGEM Corporation
The DRGME’s directive DR-QP-0708-03_DI code assignment specifies that the UDI (Unique Device Identifier) is assigned based on the system model name, power specifications, and maximum x-ray tube voltage of the x-ray tube. *Power Specification (V) / maximum tube Voltage (kV) : 200-240 V~ / 125kV
0
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GXR-ES,ECS Diagnostic X-ray System
DRGEM Corporation
The DRGME’s directive DR-QP-0708-03_DI code assignment specifies that the UDI (Unique Device Identifier) is assigned based on the system model name, power specifications, and maximum x-ray tube voltage of the x-ray tube. *Power Specification (V) / maximum tube Voltage (kV) : 200-240 V~ / 125kV
0
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GXR-ES,ECS Diagnostic X-ray System
DRGEM Corporation
The DRGME’s directive DR-QP-0708-03_DI code assignment specifies that the UDI (Unique Device Identifier) is assigned based on the system model name, power specifications, and maximum x-ray tube voltage of the x-ray tube. *Power Specification (V) / maximum tube Voltage (kV) : 200-240 V~ / 125kV
0
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GXR-ES,ECS Diagnostic X-ray System
DRGEM Corporation
The DRGME’s directive DR-QP-0708-03_DI code assignment specifies that the UDI (Unique Device Identifier) is assigned based on the system model name, power specifications, and maximum x-ray tube voltage of the x-ray tube. *Power Specification (V) / maximum tube Voltage (kV) : 200-240 V~ / 125kV
0
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GXR-ES,ECS Diagnostic X-ray System
DRGEM Corporation
The DRGME’s directive DR-QP-0708-03_DI code assignment specifies that the UDI (Unique Device Identifier) is assigned based on the system model name, power specifications, and maximum x-ray tube voltage of the x-ray tube. *Power Specification (V) / maximum tube Voltage (kV) : 200-240 V~ / 125kV
0
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GXR-ES,ECS Diagnostic X-ray System
DRGEM Corporation
The DRGME’s directive DR-QP-0708-03_DI code assignment specifies that the UDI (Unique Device Identifier) is assigned based on the system model name, power specifications, and maximum x-ray tube voltage of the x-ray tube. *Power Specification (V) / maximum tube Voltage (kV) : 200-240 V~ / 125kV
0
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GXR-ES,ECS Diagnostic X-ray System
DRGEM Corporation
The DRGME’s directive DR-QP-0708-03_DI code assignment specifies that the UDI (Unique Device Identifier) is assigned based on the system model name, power specifications, and maximum x-ray tube voltage of the x-ray tube. *Power Specification (V) / maximum tube Voltage (kV) : 200-240 V~ / 125kV
0
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uDR
Shanghai United Imaging Healthcare Co., Ltd.
Digital Medical X-ray Imaging System
0
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Z-MOTION
CONTROL-X Medical Kereskedelmi és Szolgáltató Zártkörűen Működő Részvénytársaság
Z-MOTION DIGITAL DIAGNOSTIC X-RAY SYSTEM