Cosmetic
GoodCosmetic Condition
New in box
Excellent
Good
Poor
Overview
Description:
This Hans Rudolph 5530 Series Calibration Syringe is a 3-liter calibration instrument designed for use with compatible measurement equipment. The unit provides a controlled volume for calibration and verification applications and is identified by serial number 13988.
Specifications:
Brand: Hans Rudolph
Series: 5530
Product Type: Calibration Syringe
Capacity: 3 Liters
Application: Compatible Measurement Equipment
Function: Calibration and Volume Verification
Serial Number: 13988
Features:
3-liter volume capacity
Designed for compatible calibration applications
Controlled-volume syringe design
Suitable for measurement system verification
Technical Details
| Brand | Hans Rudolph |
|---|---|
| Category | Calibration Syringe |
| Medical Discipline | Laboratory |
| Condition | Used |
| Cosmetic Condition | Good |
| OEM | Hans Rudolph |
| SKU | PIC R BOX1-4 |
| 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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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.
