Cosmetic
GoodCosmetic Condition
New in box
Excellent
Good
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Overview
BD Alaris 8100 Infusion Pump Module | Pre-Owned
Description
The BD Alaris 8100 IV Infusion Pump Module is a large-volume infusion pump module designed for use with compatible Alaris PC Units as part of the Alaris infusion system. The module is used for controlled delivery of intravenous fluids and medications in professional clinical environments.
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
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BD Alaris 8100 IV Infusion Pump Module
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Items shown in the photographs
Only the items shown in the photographs or specifically listed are included. Alaris PC Unit/controller is not included unless shown in the photographs or specifically stated. Additional accessories, cables, power supplies, manuals, software, licenses, administration sets, consumables, or other components are not included unless expressly stated.
Specifications
| Manufacturer | BD |
|---|---|
| Brand / Product Family | Alaris |
| Model | 8100 |
| Product Type | IV Infusion Pump Module |
| Configuration | Large-Volume Pump Module |
| Application | Controlled IV fluid and medication delivery |
| Compatibility | Designed for use with compatible Alaris PC Units |
| SKU | SEC BLACK S-1B |
| Intended Environment | Professional clinical, hospital, or healthcare environments |
| Return Eligibility | See product page and Return Policy |
Features
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Large-volume IV infusion pump module
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Designed for integration with compatible Alaris PC Units
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Supports controlled delivery of IV fluids and medications
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Modular design for use within the Alaris infusion system
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Model 8100 configuration
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.
Shipping & Receiving
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Professionally packaged for safe transport
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Buyer should inspect the shipment upon arrival
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Any shipping damage should be reported promptly
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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 | Infusion pump module |
| Medical Discipline | Intensive Care Unit |
| Cosmetic Condition | Good |
| OEM | CareFusion |
| SKU | SEC BLACK S-1B |
| 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.
