Powers On
YesCosmetic
GoodCosmetic Condition
New in box
Excellent
Good
Poor
Overview
Description:
The Philips IntelliBridge EC10 Interfacing Module is a medical equipment interface component designed to connect compatible external devices with supported Philips patient monitoring systems. It provides an interface for data communication and integration within compatible healthcare monitoring environments. The module is identified by reference number 865115.
Specifications:
Brand: Philips
Product Line: IntelliBridge
Model: EC10
Product Type: Interfacing Module
Reference Number: 865115
Function: Device Interface and Data Communication
Application: Compatible Patient Monitoring Systems
Features:
Philips IntelliBridge EC10 configuration
Medical equipment interfacing component
Designed for compatible Philips monitoring systems
Supports equipment integration workflows
Reference 865115
Technical Details
| Brand | Philips |
|---|---|
| Category | Interfacing Module |
| Medical Discipline | Intensive Care Unit |
| Condition | Used |
| Cosmetic Condition | Good |
| Powers On | Yes |
| OEM | Philips |
| SKU | DA41-BOX1-AC |
| Warranty | 30 - Warranty |
Need This Product Certified Patient-Ready?
If you require this product to be patient-ready certified, you can request a quote. Inspection, testing, repair, electrical safety testing, and calibration services are available through A Biomedical Service, Inc.
Safety & Biomedical Inspection Notice
Shipping & Receiving Notice
Medical equipment may require inspection, functional verification, calibration, preventive maintenance, safety testing, or other evaluations following transportation and before being placed into service.
Upon receipt, the purchaser is responsible for inspecting the equipment for any shipping damage and determining whether any inspection, testing, calibration, preventive maintenance, or certification is necessary based on the manufacturer's recommendations, the receiving facility's policies, and all applicable laws and regulations.
The equipment should not be placed into clinical service or used for patient care until the purchaser has verified that it is safe, appropriate, and compliant for its intended use.
Biomedical Inspection Notice
Medical equipment should be evaluated by qualified personnel before being placed into clinical service. Depending on the type of equipment, the evaluation may include, as applicable:
- Electrical safety testing
- Functional performance verification
- Alarm verification (if applicable)
- Battery inspection or replacement (if applicable)
- Calibration verification (if applicable)
- Preventive maintenance
- Software configuration and system settings
- Verification of compatible accessories, consumables, and disposables
- Inspection for shipping or handling damage
- Compliance with the manufacturer's recommendations
- Compliance with the receiving facility's policies, procedures, and applicable regulatory requirements
Transportation, storage, handling, and installation may affect the performance of medical equipment. Reuse Medical recommends that the receiving facility inspect, test, and evaluate the equipment in accordance with the manufacturer's recommendations and the facility's biomedical engineering procedures before placing the equipment into clinical service or patient use.
