The GE OEC 9900 Elite is designed for office‚ outpatient‚ and ambulatory centers‚ offering configurations with 12/9/6 or 9/6/4.5 image intensifier options.
Overview of the OEC Elite Platform
The OEC Elite platform represents a significant advancement in C-arm technology‚ specifically tailored for modern surgical and interventional procedures. Configurations like the 9900 Elite cater to diverse clinical settings – from busy outpatient centers to comprehensive hospital environments. This system prioritizes image quality and workflow efficiency‚ offering clinicians enhanced visualization and control during procedures.
Key to the Elite platform’s versatility are its selectable C-arm assemblies. Users can choose between the standard 12/9/6 inch (31/23/15cm) image intensifier or the Super C-arm with a 9/6/4.5 inch (23/15/11cm) intensifier‚ adapting to specific anatomical requirements and imaging needs. The system’s design also considers practical aspects like transport and cooling‚ with options for operation both with and without active cooling (requiring a 16A service for the latter).
General Electric Company continually refines the Elite platform‚ reserving the right to update specifications and features‚ ensuring it remains at the forefront of C-arm innovation.
Intended Use and Clinical Applications
The GE OEC 9900 Elite C-arm is primarily intended for use in fluoroscopic imaging applications within medical environments. Its versatile design supports a broad spectrum of clinical procedures‚ making it suitable for diverse specialties. Specifically‚ the system excels in orthopedic surgeries‚ pain management interventions‚ and vascular procedures‚ providing real-time radiographic imaging to guide clinicians.
The Elite platform’s adaptability makes it ideal for office-based‚ outpatient‚ and ambulatory center settings. Surgeons and interventionalists utilize it for minimally invasive procedures‚ benefiting from its enhanced image quality and maneuverability. Applications extend to foreign object localization‚ fracture reduction‚ and catheter placement‚ among others.
The choice between standard and Super C-arm configurations allows tailoring to specific anatomical regions and procedural complexities. Ultimately‚ the OEC Elite aims to improve diagnostic accuracy and procedural efficiency‚ contributing to enhanced patient care.
System Configurations: 9900 Elite
The GE OEC 9900 Elite platform offers adaptable configurations to meet varied clinical needs. Key options include the Standard C-arm Assembly‚ featuring a 12/9/6 inch (31/23/15cm) image intensifier (I.I.)‚ ideal for general radiographic procedures. Alternatively‚ the Super C-arm Assembly utilizes a 9/6/4.5 inch (23/15/11cm) I.I.‚ providing enhanced detail for specialized applications.
These configurations cater to different anatomical areas and procedural complexities. The larger I.I. of the Standard C-arm offers a wider field of view‚ while the Super C-arm’s smaller I.I. delivers superior resolution for intricate examinations. Both systems support mobile fluoroscopy‚ enabling real-time imaging during surgical and interventional procedures.
Considerations for configuration selection include the required image detail‚ anatomical coverage‚ and clinical workflow. Proper setup‚ including transport positioning and active cooling (requiring a 16A service)‚ is crucial for optimal performance.
System Components and Assemblies
The OEC 9900 Elite utilizes Standard and Super C-arm assemblies‚ differing in image intensifier (I.I.) sizes – 12/9/6 or 9/6/4.5 inches respectively.
Standard C-Arm Assembly (12/9/6 I.I.)
The Standard C-Arm Assembly‚ featuring a 12/9/6 inch (31/23/15cm) image intensifier (I.I.)‚ is a foundational configuration within the GE OEC 9900 Elite platform. This assembly is particularly well-suited for a broad range of diagnostic imaging procedures in office-based settings‚ outpatient clinics‚ and ambulatory surgical centers.
Its design prioritizes versatility and ease of maneuverability‚ allowing clinicians to achieve optimal image quality across diverse anatomical regions. The 12-inch I.I. provides a larger field of view‚ beneficial for visualizing larger anatomical structures‚ while the 9 and 6-inch options offer increased magnification for detailed examination of smaller areas.
Understanding the specific capabilities of this assembly‚ including its limitations regarding active cooling requirements (requiring a 16A service for implementation)‚ is crucial for safe and effective operation. Proper transport positioning‚ ensuring the system is secured‚ is also essential when moving the unit;
Super C-Arm Assembly (9/6/4.5 I.I.)
The Super C-Arm Assembly‚ equipped with a 9/6/4.5 inch (23/15/11cm) image intensifier (I.I.)‚ represents a more compact and maneuverable configuration within the GE OEC 9900 Elite series. This assembly is designed for procedures demanding precise imaging in confined spaces‚ making it ideal for specialized applications and complex cases.
The smaller I.I. sizes offer enhanced magnification capabilities‚ allowing clinicians to visualize intricate anatomical details with greater clarity. The 9-inch I.I. provides a balance between field of view and magnification‚ while the 6 and 4.5-inch options are optimized for highly detailed examinations of smaller structures.
Like the Standard assembly‚ understanding the Super C-Arm’s operational requirements‚ including potential active cooling needs (requiring a 16A service) and secure transport positioning‚ is paramount for optimal performance and patient safety. The Super 9 I.I. (23cm) is a notable component.
Image Intensifier (I.I.) Sizes and Specifications
The GE OEC 9900 Elite offers versatility through multiple Image Intensifier (I.I.) sizes‚ catering to diverse clinical needs. Standard configurations feature 12/9/6 inch (31/23/15cm) I.I. options‚ while the Super C-Arm utilizes 9/6/4.5 inch (23/15/11cm) I.I. sizes. These varying diameters directly impact the field of view and magnification capabilities.
Larger I.I.s‚ like the 12 and 9-inch‚ provide a wider anatomical view‚ suitable for general radiographic procedures. Conversely‚ smaller I.I.s (6 and 4.5-inch) deliver increased magnification‚ ideal for detailed visualization of smaller structures during specialized interventions. The Super 9 I.I. (23cm) is a frequently used option.
Understanding these specifications is crucial for selecting the appropriate I.I. for each procedure. General Electric Company retains the right to modify specifications and features‚ or discontinue models‚ so always refer to the latest documentation.
System Setup and Transport
Proper transport requires positioning the system correctly‚ ensuring it’s in the designated transport position‚ and noting active cooling needs 16A service;
Transport Position Procedures
Prior to any movement of the GE OEC Elite C-Arm system‚ adherence to strict transport position procedures is crucial for safety and preventing damage. The system must be fully configured into its designated transport position‚ a process detailed within the comprehensive user manual. This involves securing all movable components‚ including the C-arm itself‚ the workstation‚ and any attached accessories.
Specifically‚ the image intensifier should be rotated and locked into a protected orientation. All cables must be neatly coiled and secured to prevent entanglement or strain during transit. Wheel locks‚ if equipped‚ should be engaged; It’s essential to verify that the system is stable and balanced before attempting any movement;
Furthermore‚ the user manual provides detailed illustrations and step-by-step instructions for achieving the correct transport position. Ignoring these procedures could lead to equipment malfunction‚ potential injury‚ or voiding of the warranty. Always consult the manual and ensure all personnel involved in transport are thoroughly trained.
Active Cooling Requirements (16A Service)
The GE OEC Elite C-Arm systems‚ particularly during extended or high-utilization procedures‚ may require active cooling to maintain optimal performance and prevent overheating of the image intensifier. This functionality is designated as “16A Service” and necessitates a specific service installation and ongoing maintenance as outlined in the user manual.
Without active cooling‚ the system’s operational capacity can be significantly reduced‚ potentially leading to image quality degradation or even system shutdown. The manual details the environmental conditions under which active cooling is mandatory‚ including ambient temperature and procedure duration.
Installation of the 16A service involves connecting the C-arm to an appropriate cooling source‚ typically a dedicated chiller unit. Regular inspection and maintenance of the cooling system are vital‚ as specified in the service schedule within the user manual. Failure to adhere to these requirements may invalidate the warranty and compromise patient safety.
Warranty Information for Specialty Components
GE HealthCare warrants detectors‚ probes‚ tubes‚ and image intensifiers against defects in material and workmanship under normal use‚ meeting written specifications.
Defect Coverage and Performance Standards
GE HealthCare’s warranty ensures each specialty component – detectors‚ probes‚ tubes‚ and image intensifiers – is free from material and workmanship defects during normal use. Performance must substantially align with GE HealthCare’s written specifications‚ as they existed at the component’s shipping date.
This coverage extends to components exhibiting non-conformity to these established standards. However‚ the warranty explicitly excludes issues arising from improper installation‚ unauthorized modifications‚ misuse‚ or neglect. Furthermore‚ the use of non-approved parts immediately voids any warranty claims.
GE reserves the right to inspect any claimed defect and determine the appropriate course of action‚ which may include repair‚ replacement‚ or refund. The warranty’s effectiveness is contingent upon adherence to GE’s recommended maintenance schedules and operating guidelines. Documentation proving compliance may be required during the claims process.
Warranty Period and Delivery Date
The warranty for GE HealthCare specialty components initiates on the delivery date of the specific component to the customer. The duration of coverage varies depending on the component type‚ as detailed in a separate warranty table provided by GE HealthCare. It’s crucial to reference this table for precise timeframes.
This warranty period represents the timeframe during which GE HealthCare will address defects in materials or workmanship under normal use. Claims submitted after the specified warranty period expires will not be honored. Maintaining accurate delivery records is essential for validating warranty eligibility.
Customers are responsible for verifying the delivery date upon receipt of the component. Any discrepancies should be reported to GE HealthCare immediately. The warranty is non-transferable and applies solely to the original purchaser of the specialty component.
Exclusions to Warranty Coverage (Non-Approved Parts)
GE HealthCare’s warranty explicitly excludes coverage for any defects or damages resulting from the use of parts or components not expressly approved in writing by GE HealthCare. Utilizing non-approved components immediately voids the warranty for the affected specialty component and potentially related systems.
This exclusion is in place to safeguard the integrity and performance of GE HealthCare equipment. Non-approved parts may not meet the stringent quality standards required for safe and reliable operation‚ potentially leading to system malfunctions or patient safety concerns.
Customers are strongly advised to only use genuine GE HealthCare replacement parts or components authorized by GE HealthCare; Any modifications or repairs performed with non-approved parts are undertaken at the customer’s own risk. Documentation proving part approval must be readily available for warranty claims.
GE Healthcare Spin-off and Company Updates
GE Healthcare now operates as an independent company‚ alongside GE Aerospace and GE Vernova‚ following a strategic spin-off. Visit GE.com for details.
GE Aerospace‚ GE Vernova‚ and GE Healthcare
The transformation of GE into three independent‚ focused companies – GE Aerospace‚ GE Vernova‚ and GE Healthcare – marks a pivotal moment. This strategic spin-off aims to unlock greater value and agility for each business. GE Aerospace‚ now a standalone public company‚ is investing over $650 million in manufacturing and supply chain enhancements.
GE Vernova is poised to lead in the energy transition‚ while GE Healthcare continues to innovate in medical technology. These changes reflect GE’s commitment to empowering the next generation through specialized expertise. The updated GE.com website now serves as the central hub for information on all three companies.
Customers‚ employees‚ and investors can find frequently asked questions addressing the spin-off on the respective company websites. GE’s 2023 Annual Report and 10-K provide further insights into this evolution and the future direction of each entity.
Accessing Updated Company Information (GE.com)
GE.com has undergone a significant update to reflect the separation into three independent entities: GE Aerospace‚ GE Vernova‚ and GE Healthcare. The website now functions as a portal‚ directing users to the dedicated standalone sites for each company. This restructuring ensures focused information access for customers‚ investors‚ and employees navigating the transition.
For detailed information on GE Aerospace‚ visit their specific website to explore their advancements in aviation technology and manufacturing investments. Similarly‚ GE Vernova’s site provides insights into their energy solutions and commitment to a sustainable future. GE Healthcare’s platform showcases their latest medical innovations and healthcare technologies.
The spin-off’s completion marks a new chapter for GE‚ and these updated websites are crucial resources for understanding the individual strategies and future outlook of each company. Accessing these sites provides the most current and relevant information.
