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Overview
Qualitron DW-41 Mini Micro Centrifuge 115V/60HZ S/N 009152
Description
The Qualitron DW-41 is a compact mini microcentrifuge designed for compatible laboratory sample processing. This unit is identified as serial number 009152 and has a 115V, 60Hz power configuration.
What's Included
- One Qualitron DW-41 Mini Micro Centrifuge 115V/60HZ S/N 009152 unit
Only the items shown or expressly listed are included.
Specifications
| Manufacturer | Qualitron |
|---|---|
| Model / Reference | DW-41 |
| Product Type | Mini Microcentrifuge |
| Power Rating | 115V, 60Hz |
| Serial Number | 009152 |
| Configuration | Compact benchtop unit |
Features
- Compact mini microcentrifuge design
- Benchtop laboratory configuration
- 115V, 60Hz electrical rating
- DW-41 model configuration
Condition
Pre-owned laboratory equipment. Cosmetic signs of prior use and handling may be present. Review the product images for the overall appearance and included components.
Shipping & Receiving
- Review the shipping options and charges provided with the order.
- Inspect the shipment upon arrival and report transit damage promptly.
- Follow your facility's equipment inspection and setup procedures before use.
Return Eligibility
Return eligibility is subject to the current Reuse Medical Equipment Return & Refund Policy.
Technical Details
| Brand | Qualitron |
|---|---|
| Category | Mini Micro Centrifuge |
| Medical Discipline | Laboratory |
| Condition | For Parts |
| Cosmetic Condition | Good |
| OEM | Qualitron |
| SKU | METAL SHELF-27 |
| 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.
Related Products
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.
