Powers On
YesCosmetic
GoodCosmetic Condition
New in box
Excellent
Good
Poor
Overview
Description:
The Joerns Dolphin Fluid Immersion Simulation Mattress Therapy System Pump is an equipment component designed for use with compatible Joerns Dolphin mattress therapy systems. Its pump configuration supports the operation of the associated mattress system by providing the required air circulation and system control functions. The unit is intended for integration into compatible patient support equipment setups within healthcare and clinical environments.
Specifications:
Brand: Joerns
Product Line: Dolphin
Product Type: Mattress Therapy System Pump
Equipment Type: Therapy System Pump
System Type: Fluid Immersion Simulation
Function: Air Circulation and System Operation
Component Type: Pump Unit
Application: Compatible Joerns Dolphin Mattress Systems
Features:
Dolphin therapy system pump configuration
Designed for compatible Joerns mattress systems
Air circulation functionality
Patient support equipment component
Suitable for healthcare equipment environments
Technical Details
| Brand | Joerns |
|---|---|
| Category | Mattress Therapy System Pump |
| Medical Discipline | Physical Therapy |
| Condition | Used |
| Cosmetic Condition | Good |
| Powers On | Yes |
| OEM | Joerns |
| SKU | DA43-ITEM-L |
| 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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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.
