Powers On
Not ApplicableFunctional
Fully FunctionalCosmetic
GoodFunctional Condition
New
Used
Non-functional
Biomed Certified
Cosmetic Condition
New in box
Excellent
Good
Poor
Overview
Description:
This Olympus WA03200A S Fiber Optic Light Cable is a high-quality endoscopic accessory designed to transmit illumination from a compatible light source to compatible endoscopic instruments. It provides efficient optical light transmission and is suitable as a replacement light cable for compatible Olympus endoscopic systems.
Specifications:
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Brand: Olympus
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Model: WA03200A S
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Product Type: Fiber Optic Light Cable
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Component Type: Endoscopic Light Cable
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Function: Light Transmission
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Application: Compatible Olympus Endoscopic Systems
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Construction: Flexible Fiber Optic Cable
Features:
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High-quality fiber optic light transmission
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Designed for compatible Olympus endoscopic systems
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Flexible and durable cable construction
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Provides reliable illumination for compatible endoscopic instruments
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OEM endoscopic accessory
Technical Details
| Brand | Olympus |
|---|---|
| Category | Fiber Optic Light Cable |
| Medical Discipline | General Surgery |
| Condition | Used |
| Functional Condition | Fully Functional |
| Cosmetic Condition | Good |
| Powers On | Not Applicable |
| OEM | Olympus |
| SKU | DA24-A26 |
| 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.
