Powers On
YesCosmetic
GoodCosmetic Condition
New in box
Excellent
Good
Poor
Overview
Description:
The Bruker e-scan E-BOX II EPR Spectrometer Electronic Unit P/N E2043000 is an electronic equipment component designed for use with compatible Bruker e-scan Electron Paramagnetic Resonance (EPR) spectroscopy systems. Its electronic unit configuration serves as part of the spectrometer system architecture, supporting communication and electronic functions within compatible equipment setups. It is intended for integration into suitable laboratory spectroscopy and research environments.
Specifications:
Brand: Bruker
Product Line: e-scan
Model: E-BOX II
Part Number: E2043000
Product Type: EPR Spectrometer Electronic Unit
Equipment Type: Spectroscopy System Component
Technology: Electron Paramagnetic Resonance (EPR)
Function: Spectrometer Electronic System Operation
Application: Laboratory Spectroscopy / Research
Features:
E-BOX II electronic unit configuration
Designed for compatible Bruker e-scan systems
EPR spectroscopy equipment component
Electronic system integration design
Suitable for laboratory research environments
SKU : ROW-3-109
Technical Details
| Brand | Bruker |
|---|---|
| Category | EPR Spectrometer Electronic Unit |
| Condition | Used |
| Cosmetic Condition | Good |
| Powers On | Yes |
| OEM | Bruker |
| SKU | ROW-3-109 |
| 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.
