Powers On
YesCosmetic
GoodCosmetic Condition
New in box
Excellent
Good
Poor
Overview
Description:
The Given Imaging A120 ManoScan High Resolution Manometry (HRM) Module Ref FGS-4374 is a medical equipment module designed for use with compatible ManoScan systems. It is part of a high-resolution manometry equipment configuration used in gastrointestinal pressure measurement applications. Its modular design allows integration with compatible system components in suitable clinical and diagnostic environments.
Specifications:
Brand: Given Imaging Inc
Model: A120
Product Line: ManoScan
Reference Number: FGS-4374
Product Type: High Resolution Manometry Module
Technology: High Resolution Manometry (HRM)
Function: Gastrointestinal Pressure Measurement
Application: Gastrointestinal Diagnostics
Equipment Type: Manometry System Module
Features:
High-resolution manometry module design
ManoScan system configuration
Designed for compatible Given Imaging equipment
Modular equipment integration
Intended for gastrointestinal diagnostic applications
Technical Details
| Brand | Given Imaging Inc |
|---|---|
| Category | High Resolution Manometry Module |
| Medical Discipline | Internal Medicine |
| Condition | Used |
| Cosmetic Condition | Good |
| Powers On | Yes |
| OEM | Given Imaging Inc. |
| SKU | ROW-3-100 |
| 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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No similar items available.
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.
