Powers On
YesCosmetic
GoodCosmetic Condition
New in box
Excellent
Good
Poor
Overview
Description:
The Grass Instruments S12 Isolated Biphasic Stimulator is an electrophysiology instrument designed for use in compatible laboratory research and experimental setups. This unit features an isolated biphasic stimulation configuration for generating controlled electrical stimulus signals in electrophysiology applications. Its design supports integration with compatible laboratory instruments and research equipment used in electrical stimulation studies. Operating on a 115V electrical input, this unit is intended for suitable electrophysiology and laboratory research environments.
Specifications:
Brand: Grass Instruments
Model: S12
Product Type: Isolated Biphasic Stimulator
Equipment Type: Electrophysiology Unit
Stimulation Type: Biphasic
Output Configuration: Isolated
Function: Electrical Signal Stimulation
Voltage: 115V
Application: Electrophysiology / Laboratory Research
Features:
Isolated biphasic stimulation configuration
Designed for electrophysiology applications
Controlled electrical stimulus generation
Laboratory instrument integration
115V electrical input
Suitable for compatible research equipment setups
Technical Details
| Brand | Grass Instruments |
|---|---|
| Category | Isolated Biphasic Stimulator |
| Medical Discipline | Biological Laboratory |
| Condition | Used |
| Cosmetic Condition | Good |
| Powers On | Yes |
| OEM | Grass Instruments |
| SKU | DA451-ITEM-HH |
| 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.
