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Olympus

Regular price $1,249.99 USD
Regular price Sale price $1,249.99 USD
Sale Sold out

Condition: Used

Warranty: 30 - Warranty

OEM: Olympus

SKU#: DA24-A32

Quantity
Duties included. Shipping calculated at checkout.

For sale to qualified healthcare professionals, healthcare facilities, biomedical service organizations, and authorized purchasers only. This listing does not include medication, pharmaceuticals, syringes, needles, or prescription drugs.

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Powers On

Not Applicable

Functional

Tested / Working

Cosmetic

Good

Functional Condition

New

Used

Non-functional

Biomed Certified

Cosmetic Condition

New in box

Excellent

Good

Poor

Condition ratings are based on a visual inspection and functional testing when possible.

Overview

Description:

This Olympus A22002A 30° Autoclave Cystoscope is a precision rigid endoscopic instrument designed for use with compatible Olympus cystoscopic systems. Featuring a 30° direction of view, it provides high-quality optical visualization for compatible endoscopic procedures. Its autoclavable construction supports standard sterilization processes, making it suitable as a replacement instrument for compatible systems.

Specifications:

  • Brand: Olympus

  • Model: A22002A

  • Product Type: Autoclave Cystoscope

  • Viewing Angle: 30°

  • Instrument Type: Rigid Endoscope

  • Function: Optical Visualization

  • Application: Compatible Olympus Cystoscopic Systems

  • Construction: Medical-Grade Metal and Optical Glass

  • Sterilization: Autoclavable

Features:

  • Precision optical 30° cystoscope

  • Autoclavable construction for repeated sterilization

  • Designed for compatible Olympus cystoscopic systems

  • High-quality optical visualization

  • OEM endoscopic optical instrument

Technical Details

BrandOlympus
CategoryAutoclave Cystoscope
Medical DisciplineGeneral Surgery
ConditionUsed
Functional ConditionTested / Working
Cosmetic ConditionGood
Powers OnNot Applicable
OEMOlympus
SKUDA24-A32
Warranty30 - 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.

ISO 9001:2015
ISO 14001:2015
ISO 45001:2018
👉 Learn more about the equipment certification process
⚠️ 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.