Powers On
YesCosmetic
GoodCosmetic Condition
New in box
Excellent
Good
Poor
Overview
Description:
The Mindray Datascope Accutorr Plus Patient Monitor Ref 0998-00-0444-93A is a compact monitoring system designed for use in compatible healthcare and clinical environments. Its Accutorr Plus configuration provides a platform for monitoring selected patient vital sign parameters. The system is designed for integration into suitable medical monitoring setups and supports routine clinical observation workflows.
Specifications:
Brand: Mindray
Product Line: Datascope Accutorr Plus
Model: Accutorr Plus
Reference Number: 0998-00-0444-93A
Product Type: Patient Monitor
Equipment Type: Patient Monitoring System
Function: Vital Signs Monitoring
Application: Clinical / Healthcare Environments
Features:
Accutorr Plus monitoring system design
Compact patient monitoring configuration
Designed for clinical monitoring environments
Supports compatible monitoring accessories
Suitable for healthcare equipment setups
SKU : ROW-3-110
Technical Details
| Brand | Mindray |
|---|---|
| Category | Patient Monitor |
| Medical Discipline | Intensive Care Unit |
| Condition | Used |
| Cosmetic Condition | Good |
| Powers On | Yes |
| OEM | Mindray |
| SKU | ROW-3-110 |
| 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.
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.
