Powers On
Not ApplicableFunctional
Tested / WorkingCosmetic
GoodFunctional Condition
New
Used
Non-functional
Biomed Certified
Cosmetic Condition
New in box
Excellent
Good
Poor
Overview
Description:
This Olympus BF Type 1T180 EVIS EXERA II Video Gastroscope is a flexible endoscopic instrument designed for use with compatible Olympus EVIS EXERA II endoscopy systems. It provides high-quality video imaging for compatible endoscopic applications and is suitable as a replacement instrument for compatible Olympus systems.
Specifications:
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Brand: Olympus
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Model: BF Type 1T180
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Series: EVIS EXERA II
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Product Type: Video Gastroscope
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Instrument Type: Flexible Video Endoscope
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Serial Number: 2143852
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Function: Video Imaging
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Application: Compatible Olympus EVIS EXERA II Endoscopy Systems
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Construction: Medical-Grade Materials
Features:
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High-quality video imaging
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Compatible with Olympus EVIS EXERA II systems
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Flexible endoscope design
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Precision OEM endoscopic instrument
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Durable medical-grade construction
Technical Details
| Brand | Olympus Medical Systems |
|---|---|
| Category | Video Gastroscope |
| Medical Discipline | General Surgery |
| Condition | Used |
| Functional Condition | Tested / Working |
| Cosmetic Condition | Good |
| Powers On | Not Applicable |
| OEM | Olympus |
| SKU | AB4-15(4) |
| 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.
