Powers On
YesCosmetic
GoodCosmetic Condition
New in box
Excellent
Good
Poor
Overview
Description:
The Silent Solution Silencer 2100 Centrifuge System, model S2100, is a laboratory centrifuge designed for sample processing in compatible laboratory environments. The system operates on a 117V power supply at 60Hz and is intended for laboratory workflows that require centrifugal separation. Its model designation supports identification within laboratory equipment inventories.
Specifications:
Brand: The Silent Solution
Model: S2100
Product Line: Silencer 2100
Product Type: Centrifuge System
Power Requirement: 117V
Frequency: 60Hz
Function: Centrifugal Sample Processing
Application: Laboratory Workflows
Features:
Silencer 2100 system configuration
Designed for laboratory centrifugation workflows
117V electrical operation
60Hz power frequency
Model S2100
Technical Details
| Brand | The Silent Solution |
|---|---|
| Category | Centrifuge System |
| Medical Discipline | Laboratory |
| Condition | Used |
| Cosmetic Condition | Good |
| Powers On | Yes |
| OEM | The Silent Solution |
| SKU | UPSTAIRS-2-9 |
| 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.
