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 Germany A42091A Hystero-Resectoscope Working Insert is designed for use with compatible endoscopic instrument systems. It serves as a precision mechanical working insert for hystero-resectoscope assemblies and is supplied with a Richard Wolf 8570.010 sterilization tray for secure storage, organization, and instrument processing.
Specifications:
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Brand: Olympus
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Model: A42091A
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Product Type: Hystero-Resectoscope Working Insert
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Component Type: Working Insert
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Function: Endoscopic Instrument Component
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Included Accessory: Richard Wolf 8570.010 Sterilization Tray
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Application: Compatible Hystero-Resectoscope Systems
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Material: Medical-Grade Metal Construction
Features:
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Designed for compatible Olympus hystero-resectoscope systems
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Precision mechanical working insert assembly
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Includes Richard Wolf 8570.010 sterilization tray
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Durable medical-grade metal construction
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OEM endoscopic instrument component
Technical Details
| Brand | Olympus |
|---|---|
| Category | Hystero-Resectoscope Working Insert |
| Medical Discipline | General Surgery |
| Condition | Used |
| Functional Condition | Fully Functional |
| Cosmetic Condition | Good |
| Powers On | Not Applicable |
| OEM | Olympus |
| SKU | AF5/2-A3 |
| 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.
