Powers On
YesCosmetic
GoodCosmetic Condition
New in box
Excellent
Good
Poor
Overview
CareFusion Alaris PCA Module Ref 8120TDXEN933 | Pre-Owned
Description
The CareFusion Alaris PCA Module Ref 8120TDXEN933 is listed in the PCA infusion pump module category for compatible equipment connection, power, service, or replacement use. The manufacturer, model, configuration, and included components are based on the product title, available listing information, and photographs.
This is pre-owned equipment. Unless otherwise noted, the equipment is intended for professional use and should be inspected, tested, and evaluated by qualified personnel before being placed into service.
What's Included
- CareFusion Alaris PCA Module Ref 8120TDXEN933
- Items shown in the photographs
Only the items shown in the photographs or specifically listed are included. Additional accessories, cables, controllers, processors, power supplies, manuals, software, licenses, consumables, or other components are not included unless expressly stated.
Specifications
| Manufacturer | CareFusion |
|---|---|
| Model | 8120TDXEN933 |
| Model / Reference | 8120TDXEN933 |
| Product Type | PCA infusion pump module |
| Configuration | PCA infusion pump module |
| Application | Compatible equipment connection, power, service, or replacement use |
| SKU | MIDDLE MAIN2-40B |
| Intended Environment | Professional technical, service, clinical, laboratory, or biomedical environments |
| Return Eligibility | See product page and Return Policy |
Features
- PCA infusion pump module configuration
- Intended for compatible equipment connection, power, service, or replacement use
- Identified model/reference: 8120TDXEN933
Condition
This item is pre-owned and may show cosmetic signs of normal prior use, including light scratches, scuffs, label wear, discoloration, or other minor handling marks.
This item is not represented as brand new. Please review all photographs carefully for the item's actual cosmetic condition and included components.
Testing Performed
Power-on status: Confirmed.
No additional functional, calibration, accuracy, or compatibility testing is represented unless specifically stated on the product page.
Shipping & Receiving
- Professionally packaged for safe transport
- Buyer should inspect the shipment upon arrival
- Any shipping damage should be reported promptly
- Equipment should be inspected and tested before being placed into service in accordance with the receiving facility's policies
Return Eligibility
See the product page for the applicable return period.
The return window for this item is stated on the product page. See the full Return & Refund Policy at reusemedicalequipment.com for details regarding eligibility, RMA requirements, and shipping responsibility.
Technical Details
| Brand | CareFusion |
|---|---|
| Category | PCA infusion pump module |
| Medical Discipline | Intensive Care Unit |
| Cosmetic Condition | Good |
| Powers On | Yes |
| OEM | CareFusion |
| SKU | MIDDLE MAIN2-40B |
| 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.
