Powers On
YesCosmetic
GoodCosmetic Condition
New in box
Excellent
Good
Poor
Overview
Description:
The Censis Censitrac Instrument Marking Digital Etching Engraving Unit is a specialized marking system designed for identification and labeling of medical instruments. Its digital etching and engraving functionality provides a method for applying identification markings to compatible instrument surfaces. The system is intended for use in medical equipment processing environments where instrument identification and tracking are part of routine organizational workflows.
Specifications:
Brand: Censis
Product Line: Censitrac
Product Type: Digital Instrument Marking Unit
Equipment Type: Etching and Engraving System
Technology: Digital Marking
Function: Instrument Identification and Marking
Application: Medical Instrument Processing
System Type: Instrument Marking Equipment
Features:
Digital etching and engraving design
Designed for medical instrument identification
Instrument marking functionality
Suitable for compatible instrument surfaces
Intended for medical equipment processing environments
Technical Details
| Brand | Censis |
|---|---|
| Category | Digital Instrument Marking Unit |
| Condition | Used |
| Cosmetic Condition | Good |
| Powers On | Yes |
| OEM | Censis Technologies |
| SKU | ROW-3-102 |
| 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.
