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Overview
Verathon BladderScan BVI 9400 Portable Bladder Scanner with Rechargeable Battery | For Parts / Repair
Description
The Verathon BladderScan BVI 9400 Portable Bladder Scanner with Rechargeable Battery is listed in the Laboratory & Diagnostic Equipment category for laboratory, research, or diagnostic use. The manufacturer, model, configuration, and included components are based on the product title, available listing information, and photographs.
This item is offered for parts, repair, or technical evaluation. It should be inspected and evaluated by qualified personnel before repair, installation, or reuse.
What's Included
- Verathon BladderScan BVI 9400 Portable Bladder Scanner with Rechargeable Battery
- Items shown in the photographs
Only the items shown in the photographs or specifically listed are included. Additional accessories, cables, controllers, processors, power supplies, manuals, software, licenses, consumables, or other components are not included unless expressly stated.
Specifications
| Manufacturer | Verathon |
|---|---|
| Model | 9400 |
| Model / Reference | BVI 9400 |
| Product Type | Laboratory & Diagnostic Equipment |
| Configuration | Portable Rechargeable Laboratory & Diagnostic Equipment |
| Application | Laboratory, research, or diagnostic use |
| SKU | MM Right 19 |
| Intended Environment | Professional laboratory, research, technical, or biomedical environments |
| Return Eligibility | See product page and Return Policy |
Features
- Laboratory & Diagnostic Equipment configuration
- Portable format
- Rechargeable design
- Portable Rechargeable Laboratory & Diagnostic Equipment
- Intended for laboratory, research, or diagnostic use
- Identified model/reference: 9400
Condition
This item is offered for parts or repair and may be incomplete, damaged, non-functional, or unsuitable for immediate use. Cosmetic wear, missing components, and other defects may be present.
Please review all photographs carefully for the item's actual condition and included components. No operational functionality is represented.
Shipping & Receiving
- Professionally packaged for safe transport
- Buyer should inspect the shipment upon arrival
- Any shipping damage should be reported promptly
- Equipment should be inspected and tested before being placed into service in accordance with the receiving facility's policies
Return Eligibility
See the product page for the applicable return period.
The return window for this item is stated on the product page. See the full Return & Refund Policy at reusemedicalequipment.com for details regarding eligibility, RMA requirements, and shipping responsibility.
Technical Details
| Brand | Verathon |
|---|---|
| Category | Laboratory & Diagnostic Equipment |
| Medical Discipline | Laboratory |
| Condition | For Parts |
| Cosmetic Condition | Good |
| OEM | Verathon |
| SKU | MM Right 19 |
| 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.
