Powers On
YesCosmetic
GoodCosmetic Condition
New in box
Excellent
Good
Poor
Overview
Description:
This Philips 3D9-3V Convex Array 3D Endocavity Ultrasound Transducer Probe is an imaging system component designed for use with compatible Philips ultrasound equipment. Featuring a convex array configuration and 3D imaging capability, it provides a specialized probe design for compatible imaging system applications.
Specifications:
Brand: Philips
Model: 3D9-3V
Product Type: Ultrasound Transducer Probe
Probe Type: Convex Array
Configuration: 3D Endocavity
Application: Compatible Philips Imaging Systems
Function: Imaging System Component
Design: Endocavity Probe
Features:
Convex array configuration
3D imaging capability
Endocavity probe design
Compact transducer configuration
Technical Details
| Brand | Philips |
|---|---|
| Category | Ultrasound Transducer Probe |
| Medical Discipline | Internal Medicine |
| Condition | Used |
| Cosmetic Condition | Good |
| Powers On | Yes |
| OEM | Philips |
| SKU | CIR-R4/2-1A |
| 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.
