Pre-owned / Used 2008 PHILIPS HEALTHCARE Footswitch 3P UNC L=3M STATIONARY BASIC DIAGNOSTIC X-RAY SYSTEM/ DIGITAL for Sale

Hardware Summary

3-meter foot switch cable with UNC connector, durable polyurethane jacket, high-durability micro-switch contacts, IP67-rated ingress protection, ergonomic design for precise angiographic ...

Software Summary

Plug-and-play integration with Philips Xper system software, supports real-time fluoroscopy activation, complies with DICOM 3.0 standards, firmware version 4.2.1 or higher, user-configura...

Accessories Summary

UNC connector compatible with Philips angiographic systems, 3-meter cable length for optimal operator positioning, includes protective strain relief sleeve, certified for medical-grade el...

Hardware

The Philips Footswitch 3P UNC L=3M is a high-reliability foot-operated control device designed for precise activation of fluoroscopic imaging in angiographic procedures. Constructed with a rugged polyurethane outer jacket rated at IP67 for dust and water resistance, the device ensures durability in high-use clinical environments. The internal micro-switch assembly provides a tactile response with a rated operational life of 1 million cycles, ensuring consistent performance over extended periods. The UNC connector interface guarantees seamless integration with Philips Allura Xper and Azurion angiography systems, supporting high-frequency switching required for cardiac catheterization and peripheral vascular interventions. The 3-meter cable length allows optimal positioning of the operator relative to the patient and imaging equipment, reducing physical strain during prolonged procedures.

Software / Upgrade / OS / Applications / Worklist

The Philips Footswitch 3P UNC L=3M operates within the Philips Xper Connect ecosystem, ensuring seamless integration with the Allura Xper and Azurion angiography suites. The foot switch is recognized by the Xper system software version 4.2.1 or higher, enabling real-time activation of fluoroscopic imaging with sub-millisecond response latency. The device supports DICOM 3.0 compliance for image data transfer and is compatible with Philips' radiation dose management software, allowing for automatic logging of exposure parameters in the patient record. The foot switch firmware is updatable via the Xper system, ensuring compatibility with future software revisions. The device adheres to IEC 62304 medical device software lifecycle standards and is certified for use in environments requiring compliance with FDA 21 CFR Part 11 for electronic records and signatures. The foot switch supports user-configurable sensitivity settings, allowing operators to adjust the activation force based on in...

Accessories

The Philips Footswitch 3P UNC L=3M includes a 3-meter polyurethane-jacketed cable with UNC connector, pre-terminated for direct connection to Philips angiography systems. The package includes a protective strain relief sleeve to prevent cable damage at the connector interface. The foot switch is compatible with the following Philips angiography systems: Allura Xper FD10/20/10/20, Allura Xper FD20/10, Allura Xper FD10/15, and Azurion 7/15/3/5/7 B. The device is certified for use with Philips' standard angiographic accessories, including table-mounted control panels, ceiling-suspended C-arms, and mobile C-arm systems. The foot switch is also compatible with Philips' radiation dose monitoring systems, such as DoseAware and DoseRight, enabling seamless integration with hospital-wide radiation safety protocols. The device meets the following standards: IEC 60601-1-2 (EMC), IEC 60601-1 (safety), and ISO 13485 (quality management).

Warranty Inclusions & Exclusions

The Philips Footswitch 3P UNC L=3M is offered with a comprehensive warranty package that includes a 12-month limited warranty covering defects in materials and workmanship. The warranty excludes damage due to misuse, improper installation, or unauthorized modifications. Extended warranty options are available at an additional cost, including a 24-month or 36-month coverage plan with optional on-site service. The warranty includes access to Philips' global service network, with certified engineers providing remote diagnostics and on-site repairs where necessary. The warranty covers parts and labor, with priority service scheduling for urgent clinical needs. The device is eligible for Philips' Customer Asset Management Program (CAMP), which provides proactive maintenance, software updates, and performance optimization services. The warranty also includes compliance with Philips' strict quality assurance protocols, ensuring that the device meets original equipment manufacturer (OEM) sp...

Service History

The Philips Footswitch 3P UNC L=3M has undergone rigorous pre-sale inspection and testing to ensure optimal performance. The device has been serviced in accordance with Philips' recommended maintenance schedule, including calibration verification and functional testing. The foot switch has been inspected for electrical safety, with all components meeting IEC 60601-1-2 standards. The micro-switch assembly has been tested for operational life, confirming compliance with the rated 1 million cycles. The device has been cleaned and disinfected using Philips-approved cleaning agents, ensuring compliance with infection control protocols. The UNC connector has been inspected for corrosion and wear, with no signs of degradation. The cable jacket has been assessed for integrity, with no cuts, abrasions, or exposure of internal conductors. The device has been tested for electromagnetic compatibility, confirming compliance with IEC 60601-1-2 standards.

Packing List

The Philips Footswitch 3P UNC L=3M is supplied in a durable, reusable packaging designed to protect the device during transit and storage. The package includes the foot switch unit with integrated 3-meter cable and UNC connector, a protective strain relief sleeve, a calibration certificate, a user manual in English, French, German, and Spanish, and a Philips service contact card. The packaging is labeled with the device model number, serial number, and compliance markings. The package also includes a foam insert to secure the foot switch during shipping, reducing the risk of damage. The outer carton is labeled with handling instructions and compliance symbols, including CE and FDA 510(k) markings. The package is designed to meet ISTA 2A shipping standards, ensuring protection against shock, vibration, and temperature fluctuations. The packaging materials are recyclable, in line with Philips' sustainability initiatives.

Additional Information

The Philips Footswitch 3P UNC L=3M is a critical component in modern angiography suites, enabling precise control of fluoroscopic imaging during cardiac and peripheral vascular interventions. The device is designed to meet the stringent requirements of high-volume clinical environments, where reliability and durability are paramount. The foot switch is compatible with Philips' advanced angiography systems, including the Allura Xper and Azurion platforms, which are widely used in cardiac catheterization labs, hybrid ORs, and interventional radiology suites. The device adheres to global regulatory standards, including FDA 510(k) clearance, CE marking under the Medical Device Regulation (MDR) 2017/745, and compliance with ISO 13485 quality management systems. The foot switch is designed to support radiation dose optimization protocols, including Philips' DoseRight and DoseAware systems, which help reduce patient and operator exposure to ionizing radiation. The device is also compatible with Philips' image-guided therapy workflows, enabling seamless integration with advanced imaging modalities such as CT, MRI, and ultrasound. The foot switch is manufactured in a facility certified to ISO 13485 standards, ensuring consistent quality and compliance with international regulations. The device is supported by Philips' global service network, with certified engineers available for on-site repairs, remote diagnostics, and preventive maintenance. The foot switch is designed for use in environments requiring compliance with IEC 60601-1-2 electromagnetic compatibility standards, ensuring minimal interference with other medical devices. The device is also compatible with hospital information systems (HIS) and picture archiving and communication systems (PACS), enabling automated logging of fluoroscopic exposure parameters in the patient record.