Cosmetic
GoodCosmetic Condition
New in box
Excellent
Good
Poor
Overview
CSZ Gentherm Blanketrol III Model 233 Hyper-Hypothermia System | Pre-Owned
Description
The CSZ Gentherm Blanketrol III Model 233 Hyper-Hypothermia System is a professional patient temperature management unit designed for compatible clinical and biomedical environments. The unit shown features separate WATER and PATIENT displays, manual and automatic control sections, temperature adjustment controls, Gradient 10C, Gradient Variable, Smart, Monitor Only, Silence Alarm, and Test Indicators controls.
This item appears to be pre-owned and shows visible cosmetic wear from prior handling or use. No power-on or functional testing information was provided with the submitted photograph, so operational status is not represented unless confirmed separately.
What's Included
- CSZ Gentherm Blanketrol III hyper-hypothermia unit shown in the photograph
- Visible power cord/cable shown with the unit
- Items shown in the photograph
Only the items shown in the photographs or specifically listed are included. Blankets, hoses, patient probes, manuals, accessories, consumables, and other components are not included unless expressly shown or stated.
Specifications
| Manufacturer / Brand | CSZ / Gentherm |
|---|---|
| Product Line | Blanketrol III |
| Model | 233 |
| Product Type | Hyper-Hypothermia Temperature Management System |
| Visible Controls | Manual Control, Auto Control, Temp Set, Gradient 10C, Gradient Variable, Smart, Monitor Only, Silence Alarm, Test Indicators |
| Application | Professional patient temperature management |
| Testing Status | Not provided / not verified |
| Intended Environment | Professional medical, clinical, hospital, or biomedical environments |
| Return Eligibility | See product page and Return Policy |
Features
- Blanketrol III temperature management platform
- Water and patient temperature display areas
- Manual and automatic control modes
- Gradient 10C and Gradient Variable controls
- Smart and Monitor Only controls
- Floor-standing professional medical equipment configuration
Condition
This item appears pre-owned. The housing and control panel show visible cosmetic wear, marks, and discoloration consistent with prior handling or use. Please review all photographs carefully for the actual cosmetic condition and included components.
Testing
No functional, calibration, or power-on testing information was provided. The unit should be inspected, tested, and approved by qualified personnel before installation or use.
Shipping & Receiving
- Professional equipment may require special handling and freight packaging
- 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 | CSZ / Gentherm |
|---|---|
| Category | Hyper-Hypothermia Temperature Management System |
| Medical Discipline | Intensive Care Unit |
| Condition | Used |
| Cosmetic Condition | Good |
| OEM | CSZ / Gentherm |
| SKU | c_red-1 |
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.
