Powers On
YesCosmetic
GoodCosmetic Condition
New in box
Excellent
Good
Poor
Overview
Description:
The Bio-Rad 1000 Mini Chiller Laboratory Refrigerated Cooling Module, Catalog Number 170-3654, is a laboratory cooling unit designed to provide temperature-controlled cooling for compatible laboratory equipment and systems. Its refrigerated cooling configuration supports laboratory applications that require a consistent cooling source during equipment operation and research workflows. The compact module is designed for integration with compatible Bio-Rad laboratory systems, making it suitable for laboratory and research environments where controlled cooling is required.
Specifications:
Brand: Bio-Rad
Model: 1000 Mini Chiller
Catalog Number: 170-3654
Product Type: Laboratory Refrigerated Cooling Module
Equipment Type: Laboratory Cooling Equipment
Cooling Type: Refrigerated Cooling
Function: Temperature-Controlled Cooling
Application: Laboratory Research / Laboratory Equipment Cooling
Features:
Refrigerated laboratory cooling configuration
Compact mini chiller design
Designed for compatible Bio-Rad equipment
Temperature-controlled cooling functionality
Laboratory equipment integration
Suitable for laboratory and research environments
Technical Details
| Brand | Bio-Rad |
|---|---|
| Category | Laboratory Refrigerated Cooling Module |
| Medical Discipline | Biological Laboratory |
| Condition | Used |
| Cosmetic Condition | Good |
| Powers On | Yes |
| OEM | Bio-Rad |
| SKU | DA434-ITEM-FF |
| 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.
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.
