Germany - angiography equipment

Description

A biplanes (2-level) angiography system with special functions for neuroradiology, the latest generation of devices, i.e. state of the art in science and technology, with accessories and additional devices (e.g. contrast medium injector, ultrasound system) is required. In addition to the floor-standing and ceiling-mounted C-arm systems, the overall system in the examination room also includes a patient support table, a ceiling rail system including support arm systems for the various components, a large-screen monitor for the connection of external signals, 1 OR light, 2 upper-body and 2 lower-body radiation shields. For the control room, all computers, operating consoles incl. keyboards, mice and monitors (also a large-screen monitor) belonging to the system are to be offered incl. brackets. An intercom system between the examination room and the control room as well as a UPS system on the device side to secure the image system, the device and table movement are part of the system. The angiography device including accessories must be suitable for fulfilling examination requirements in the area of maximum university care, e.g. neuroradiological vascular diagnostics, therapy and minimally invasive surgical procedures on lying patients are performed. Unrestricted universal angiographic diagnostics, rotational angiography, dynamic CT, modern therapeutic vascular and non-vascular intervention procedures, head/neck and thoracic/abdominal examinations as well as peripheral angiography must be possible. 2 high-resolution flat detectors with at least 40 cm diagonal in the frontal plane and 30 cm in the lateral plane are required, as well as 2 high-performance X-ray tubes for neuroradiological angiography, with special housing for constant, noiseless rotation and a technology for reducing radiation exposure. Compact depth diaphragms and 2 powerful generators with fully integrated system control and automatic regulation of radiation power for all fluoroscopy and imaging modes are part of the biplane angiography system. The standard includes the use of maximum measures to reduce the dose for patients and staff. The system must enable an efficient workflow through simple patient positioning and simple evaluation of all examination techniques. The digital imaging system shall use the latest technology and support all necessary post-processing and imaging features for all specific examinations. All coupling devices, storage aids and accessories available from the manufacturer of the system at the time of offer as a product for the Angio configuration offered shall be identified and priced. The compatibility to the devices offered in the respective lots must be marked. The system must offer standardized interfaces for the connection to a HIS/RIS/PACS system. The console and the post-processing systems available for applications must have all software options offered by the manufacturer of the system as a product at the time of commissioning that apply to the Angio configurations offered. All software options must be displayed and priced. As general contractor, the bidder is responsible for the implementation of the IT-side system connection, including the assumption of the costs incurred by third parties (e.g. RIS manufacturers) for the connection. the bidder acts as general contractor for the overall performance, which also includes the following partial services:- planning including time schedule planning for conversion in the inventory during ongoing operation,- dismantling, removal and disposal of all old equipment (including biplane Siemens Axiom Artis BA MT incl. Leonardo,- (2002) necessary structural and technical changes/adjustments. What is required is a monoplane (single-plane) multifunctional system for fluoroscopy and angiography, the latest generation of devices, i.e. based on the latest state of science and technology, including accessories and small devices (including contrast medium injector (double piston), ultrasound device).In addition to the C-arm system, the overall system in the examination room includes a system-bound patient positioning table, a ceiling rail system including support arm systems for a large-screen monitor for the connection of external signals, 2 upper body and 2 lower body beam protectors. For the control room all computers, operating consoles incl. keyboards, mice and monitors incl. brackets belonging to the system are to be offered. An intercom system between the examination room and the control room, as well as a UPS system on the device side to secure the image system, the device and table movement system component. The multifunctional system, including accessories, must be suitable for fulfilling examination requirements in the area of maximum university care. radiological diagnostics, therapy and interventional procedures on lying patients (excluding neuroradiological procedures) are performed. A high-resolution flat-panel detector in the frontal plane in approx. 20 inches is required, as is a high-performance X-ray source for angiography, with a special housing for constant, noiseless rotation and a technology for reducing radiation exposure. Compact depth diaphragm and a powerful generator with fully integrated system control and automatic regulation of radiation power for all fluoroscopy and recording modes are part of the multifunction system. The standard includes the use of maximum measures to reduce the dose for patients and staff. The system must enable an efficient workflow by simple positioning of the patient, as well as a simple evaluation of all examination techniques, if necessary also by parallel working. The digital imaging system shall use the latest technology and support all necessary post-processing and imaging features for all specific examinations. All options available from the manufacturer of the system at the time of the offer as a product for the configuration offered must be listed individually in the offer and priced and offered. the system must offer standardized interfaces for the connection to a HIS/RIS/PACS system. The console must have all software options offered by the manufacturer of the system as a product at the time of commissioning that apply to the multifunction configuration offered. All software options must be priced out individually. The bidder as general contractor is responsible for the implementation of the IT-side system connection, including the assumption of costs incurred by third parties (e.g. RIS manufacturers) for the connection. The system must have all relevant approvals in accordance with the applicable legal regulations (e.g. CE, MPG, etc.).

Opportunity closing date

20 December 2019

Value of contract

to be confirmed