Powers On
YesCosmetic
GoodCosmetic Condition
New in box
Excellent
Good
Poor
Overview
Description:
The GE Medical Systems ApexPro Quad Receiver Module is a specialized receiver assembly designed for compatible ApexPro monitoring equipment. It operates within the 560–614 MHz frequency range and is identified by reference number 419525-004.
Specifications:
Brand: GE Medical Systems
Product Line: ApexPro
Product Type: Quad Receiver Module
Assembly Type: Receiver Module
Frequency Range: 560–614 MHz
Reference Number: 419525-004
Configuration: Quad Receiver Assembly
Features:
GE Medical Systems ApexPro configuration
Quad receiver module design
560–614 MHz frequency range
Dedicated receiver assembly
Reference number 419525-004
Technical Details
| Brand | GE Medical Systems |
|---|---|
| Category | Quad Receiver Module |
| Medical Discipline | Intensive Care Unit |
| Condition | Used |
| Cosmetic Condition | Good |
| Powers On | Yes |
| OEM | GE Medical Systems |
| SKU | AC2 (A8) |
| 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.
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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.
