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Overview
Description:
The Parks Medical Electronics 1050-C Vascular Mini Lab is a vascular Doppler ultrasound system designed for use in compatible vascular assessment and diagnostic equipment environments. This system utilizes Doppler ultrasound technology to detect and monitor blood flow signals, supporting vascular measurement and evaluation workflows. Its integrated configuration is designed for professional medical and vascular laboratory settings, providing a dedicated platform for Doppler-based blood flow analysis.
Specifications:
Brand: Parks Medical Electronics
Model: 1050-C
Product Type: Vascular Mini Lab
Equipment Type: Vascular Doppler Ultrasound System
Technology: Doppler Ultrasound
Function: Blood Flow Signal Detection
Measurement Type: Vascular Doppler
Application: Vascular Assessment / Medical Diagnostics
Features:
Vascular Doppler ultrasound system configuration
Designed for vascular assessment applications
Doppler-based blood flow signal technology
Integrated vascular measurement platform
Suitable for compatible medical equipment environments
Dedicated vascular laboratory equipment design
Technical Details
| Brand | Parks Medical Electronics |
|---|---|
| Category | Vascular Doppler Ultrasound System |
| Medical Discipline | Cardiology |
| Condition | Used |
| Cosmetic Condition | Good |
| OEM | Parks Medical Electronics |
| SKU | DA433-ITEM-GG - 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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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.
