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Overview
Description:
The Vitacon VitaScan Portable 3D Ultrasound Bladder Scanner Probe is a component designed for use with the VitaScan bladder scanning system. It features a probe configuration associated with portable 3D ultrasound scanning equipment and is intended for use within a compatible system setup. The probe is identified by the Vitacon VitaScan product line and is presented with its carrying case and accessories as stated in the listing title.
Specifications:
Brand: Vitacon
Product Line: VitaScan
Product Type: 3D Ultrasound Bladder Scanner Probe
Component Type: Ultrasound Probe
Scanning Technology: 3D Ultrasound
System Type: Portable Bladder Scanning System
Application: Compatible Ultrasound Scanning Equipment
Configuration: Probe with Case & Accessories
Features:
Portable probe configuration
Designed for the Vitacon VitaScan system
3D ultrasound scanning technology
Bladder scanner equipment component
Compatible with the appropriate VitaScan system setup
Carrying case and accessories as stated in the title
Technical Details
| Brand | Vitacon |
|---|---|
| Category | 3D Ultrasound Bladder Scanner Probe |
| Medical Discipline | Radiology |
| Condition | Used |
| Cosmetic Condition | Good |
| OEM | Vitacon |
| SKU | DA432-ITEM-CC - P |
| 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.
