Powers On
YesCosmetic
GoodCosmetic Condition
New in box
Excellent
Good
Poor
Overview
Description:
The Drucker Diagnostics Fisherbrand Dash Flex 12 Fisher Stat Centrifuge is a compact laboratory centrifuge designed for sample processing in compatible laboratory and clinical environments. Its benchtop configuration provides a convenient setup for centrifugal separation applications, while its 100–240V power input supports a wide range of electrical configurations. The Dash Flex 12 features a compact equipment design suitable for routine laboratory workflows and sample preparation applications.
Specifications:
Brand: Drucker Diagnostics
Product Line: Fisherbrand
Model: Dash Flex 12
Product Type: Stat Centrifuge
Equipment Type: Laboratory Centrifuge
Voltage: 100–240V
Function: Centrifugal Sample Separation
Configuration: Benchtop
Application: Laboratory / Clinical Environments
Features:
Dash Flex 12 centrifuge design
Compact benchtop configuration
100–240V power input
Designed for laboratory sample processing
Suitable for compatible clinical and laboratory workflows
Technical Details
| Brand | Drucker Diagnostics |
|---|---|
| Category | Stat Centrifuge |
| Medical Discipline | Laboratory |
| Condition | Used |
| Cosmetic Condition | Good |
| Powers On | Yes |
| OEM | Drucker Diagnostics |
| SKU | DA431-ITEM-F |
| 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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No similar items available.
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.
