Cosmetic
GoodCosmetic Condition
New in box
Excellent
Good
Poor
Overview
Description:
The Parks Medical Electronics 1050-C Vascular Mini Lab is a vascular measurement system designed for use in compatible clinical and diagnostic environments. Operating with an 8.2MHz Doppler configuration, this unit utilizes Doppler technology for vascular signal assessment and measurement applications. Its compact Mini Lab design provides an integrated equipment setup suitable for clinical vascular examination and diagnostic workflows.
Specifications:
Brand: Parks Medical Electronics
Model: 1050-C
Product Type: Vascular Mini Lab Doppler Unit
Equipment Type: Vascular Measurement System
Technology: Doppler
Frequency: 8.2MHz
Function: Vascular Signal Assessment
Application: Vascular Diagnostics / Clinical Environments
Features:
8.2MHz Doppler configuration
Vascular Mini Lab system design
Compact equipment configuration
Designed for vascular measurement applications
Suitable for compatible clinical environments
Technical Details
| Brand | Parks Medical Electronics |
|---|---|
| Category | Vascular Mini Lab Doppler Unit |
| Medical Discipline | Cardiology |
| Condition | For Parts |
| Cosmetic Condition | Good |
| OEM | Parks Medical Electronics |
| SKU | ROW-3-116 |
| 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.
Related Products
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.
