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Overview
Description:
The Diagnostic Ultrasound BVI 3000 Bladder Scan is a portable ultrasound-based measurement system designed for use in compatible clinical and healthcare environments. Its compact design provides a portable equipment configuration, while its ultrasound technology supports bladder volume measurement applications. The system is intended for integration into suitable clinical equipment setups and healthcare workflows.
Specifications:
Brand: Diagnostic Ultrasound
Model: BVI 3000
Product Type: Portable Bladder Scanner
Equipment Type: Ultrasound Measurement System
Technology: Ultrasound
Part Number: 0570-0090
Function: Bladder Volume Measurement
Configuration: Portable
Application: Clinical / Healthcare Environments
Features:
Portable ultrasound equipment design
BVI 3000 system configuration
Designed for bladder volume measurement applications
Compact equipment configuration
Suitable for compatible clinical environments
SKU : ROW-3-117
Technical Details
| Brand | Diagnostic Ultrasound |
|---|---|
| Category | Portable Bladder Scanner |
| Condition | For Parts |
| Cosmetic Condition | Good |
| OEM | Diagnostic Ultrasound |
| SKU | ROW-3-117 |
| 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.
