Powers On
YesCosmetic
GoodCosmetic Condition
New in box
Excellent
Good
Poor
Overview
Description:
The Molecular Devices VersaMax Tunable Absorbance Microplate Reader is a laboratory instrument designed for measuring absorbance in microplate-based applications. It is used with compatible microplate formats and laboratory systems for optical absorbance measurements. Its tunable absorbance configuration supports different measurement settings for laboratory analysis and research workflows. Operating with a universal voltage input of 100–240V and a frequency range of 50–60Hz, this instrument is designed for integration into suitable laboratory environments.
Specifications:
Brand: Molecular Devices
Model: VersaMax
Product Type: Tunable Absorbance Microplate Reader
Equipment Type: Laboratory Microplate Reader
Measurement Type: Absorbance
Technology: Optical Absorbance
Voltage: 100–240V
Frequency: 50–60Hz
Function: Microplate Absorbance Measurement
Application: Laboratory Research / Microplate Analysis
Features:
Tunable absorbance measurement configuration
Designed for compatible microplate formats
Optical measurement technology
Suitable for laboratory analysis workflows
Universal 100–240V power input
50–60Hz frequency compatibility
Technical Details
| Brand | Molecular Devices |
|---|---|
| Category | Tunable Absorbance Microplate Reader |
| Medical Discipline | Biological Laboratory |
| Condition | Used |
| Cosmetic Condition | Good |
| Powers On | Yes |
| OEM | Molecular Devices |
| SKU | DA432-ITEM-DD |
| 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.
