Powers On
YesCosmetic
GoodCosmetic Condition
New in box
Excellent
Good
Poor
Overview
Description:
The Penumbra PMX110 Portable Aspiration Vacuum Suction Pump is a compact equipment unit designed for use with compatible Penumbra aspiration systems. Its vacuum pump configuration provides suction functionality within compatible equipment setups. Featuring a portable design and a 100–115V power input with 50/60Hz frequency compatibility, this unit is intended for integration into suitable medical equipment environments.
Specifications:
Brand: Penumbra
Model: PMX110
Product Type: Portable Aspiration Vacuum Suction Pump
Equipment Type: Vacuum Pump
Configuration: Portable
Voltage: 100–115V
Frequency: 50/60Hz
Function: Vacuum Generation / Aspiration
Application: Compatible Penumbra Equipment Systems
Features:
Portable vacuum pump configuration
Aspiration system component
Designed for compatible Penumbra equipment
100–115V power input
50/60Hz frequency compatibility
Compact equipment design
Technical Details
| Brand | Penumbra |
|---|---|
| Category | Portable Aspiration Vacuum Suction Pump |
| Condition | Used |
| Cosmetic Condition | Good |
| Powers On | Yes |
| OEM | Penumbra |
| SKU | DA43-ITEM-K |
| 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.
