Overview
Zimmer Biomet IntelliCart Duo Fluid Waste Management System
Description
The Zimmer Biomet IntelliCart Duo is a mobile surgical fluid waste management system intended for operating-room and procedural environments. It uses a dual-reservoir cart configuration with an integrated touchscreen interface.
This listing covers six units represented in the supplied photographs. Product identification is based on visible branding, equipment configuration, and the supplied photographs.
What's Included
- Six Zimmer Biomet IntelliCart Duo Fluid Waste Management Systems
- Reservoir assemblies, display interfaces, tubing, poles, and components visible in the supplied photographs
Specifications
| Manufacturer | Zimmer Biomet |
|---|---|
| Model / Reference | IntelliCart Duo |
| Product Type | Surgical Fluid Waste Management System |
| Reservoir Configuration | Dual 17-liter reservoirs, 34-liter total fluid capacity |
| Quantity Listed | 6 |
| Intended Environment | Professional operating room, surgical, or procedural setting |
Features
- Dual-reservoir fluid collection configuration
- Integrated touchscreen control interface
- Top-mounted manifold and tubing connections
- Mobile cart design with casters
- Upright support poles and integrated equipment frame
Condition
This is pre-owned equipment. The exterior may show cosmetic signs of prior handling, use, transport, or storage, as pictured. Review the supplied photographs for the visible condition of the available units and included components.
Shipping & Receiving
- Freight or specialized transport is required
- Inspect the shipment promptly upon arrival
- Report shipping damage promptly
- Follow the receiving facility's equipment intake and evaluation procedures before placement into service
Return Eligibility
See the product page and store Return & Refund Policy for the applicable return period and eligibility requirements.
Technical Details
| Brand | Zimmer Biomet |
|---|---|
| Category | Fluid Waste Management System |
| Medical Discipline | General Surgery |
| OEM | Zimmer Biomet |
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.
Related Products
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.
