Powers On
YesCosmetic
GoodCosmetic Condition
New in box
Excellent
Good
Poor
Overview
Description:
The Zeiss Humphrey Systems FDT 710 Series Visual Field Analyzer is an ophthalmic testing instrument designed to assess visual field responses using frequency-doubling technology (FDT). It is intended for use in compatible eye-care and ophthalmology settings for visual field examination and related diagnostic testing workflows. The system belongs to the Humphrey Systems FDT 710 series.
Specifications:
Brand: Zeiss
Product Line: Humphrey Systems
Model / Series: FDT 710
Product Type: Visual Field Analyzer
Technology: Frequency-Doubling Technology (FDT)
Function: Visual Field Testing
Application: Ophthalmology and Eye-Care Testing
Features:
FDT visual field testing technology
Humphrey Systems series configuration
Designed for ophthalmic examination workflows
Visual field response assessment
Model series FDT 710
Technical Details
| Brand | Zeiss |
|---|---|
| Category | Visual Field Analyzer |
| Medical Discipline | Internal Medicine |
| Condition | Used |
| Cosmetic Condition | Good |
| Powers On | Yes |
| OEM | Carl Zeiss |
| SKU | UPSTAIRS-2-1 |
| 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.
