Powers On
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New in box
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Overview
Description:
The Oxford Optronix OxyFlo 2000 Microvascular Blood Perfusion Monitor is a specialized monitoring instrument designed for measuring microvascular blood perfusion using compatible optical measurement technology. Its configuration supports the assessment and monitoring of tissue blood flow in laboratory research and experimental environments. The system is designed for integration into suitable research setups requiring microvascular perfusion measurements. Operating with a universal voltage input of 110–240V at 50–60Hz, this instrument is suitable for compatible laboratory and research equipment environments.
Specifications:
Brand: Oxford Optronix
Model: OxyFlo 2000
Product Type: Microvascular Blood Perfusion Monitor
Equipment Type: Perfusion Monitoring System
Measurement Type: Microvascular Blood Perfusion
Technology: Optical Measurement
Voltage: 110–240V
Frequency: 50–60Hz
Function: Blood Perfusion Monitoring
Application: Laboratory Research / Microvascular Studies
Features:
Microvascular perfusion monitoring configuration
Designed for optical blood flow measurement applications
Specialized laboratory monitoring instrument
Suitable for compatible research equipment setups
Universal 110–240V power input
50–60Hz frequency compatibility
Designed for laboratory and research environments
Technical Details
| Brand | Oxford Optronix |
|---|---|
| Category | Microvascular Blood Perfusion Monitor |
| Condition | Used |
| Cosmetic Condition | Good |
| Powers On | Yes |
| OEM | Oxford Optronix |
| SKU | DA451-ITEM-I |
| 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.
