Powers On
YesCosmetic
GoodCosmetic Condition
New in box
Excellent
Good
Poor
Overview
Description:
The Philips M1006B Invasive Blood Pressure Measurement Module is a patient monitoring component designed for integration with compatible Philips monitoring systems. It provides an interface for invasive blood pressure measurement within supported clinical monitoring configurations. The module is identified by reference number 862277.
Specifications:
Brand: Philips
Model: M1006B
Product Type: Invasive Blood Pressure Measurement Module
Reference Number: 862277
Function: Invasive Blood Pressure Monitoring
Component Type: Patient Monitoring Module
Application: Compatible Philips Patient Monitoring Systems
Features:
Philips M1006B module configuration
Invasive blood pressure measurement interface
Designed for compatible Philips monitoring equipment
Patient monitoring system integration component
Reference 862277
Technical Details
| Brand | Philips |
|---|---|
| Category | Invasive Blood Pressure Measurement Module |
| Medical Discipline | Cardiology |
| Condition | Used |
| Cosmetic Condition | Good |
| Powers On | Yes |
| OEM | Philips |
| SKU | DA41-BOX1-AD |
| 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.
