Overview
Agilent Technologies VS Series Helium Leak Detector VS MR15
Description
The Agilent Technologies VS Series Leak Detector is a professional leak-detection instrument with an integrated control/display interface and test-port connection.
This pre-owned equipment is intended for professional laboratory, research, industrial, or technical use. Product identification is based on the visible manufacturer markings, model information, equipment labels, and supplied photographs.
What's Included
- Agilent Technologies VS Series Helium Leak Detector VS MR15
- Equipment and components visible in the supplied photographs
Specifications
| Manufacturer | Agilent Technologies |
|---|---|
| Model / Reference | VS Series / VS Leak Detector |
| Manufacturer Part Number |
VS MR15
|
| Product Type | Helium Leak Detector |
| Electrical Rating | 100/115 V AC; 7 A; single phase |
| Manufacture Date | 2017-02 |
| Country of Manufacture | Malaysia |
| Intended Environment | Professional laboratory, research, industrial, or technical environments |
Features
- VS Series leak-detector configuration
- Integrated display and control interface
- Top-mounted test-port connection
- Rear communication and exhaust connections
- Mobile equipment configuration shown in the photographs
Condition
This is pre-owned equipment. The exterior shows cosmetic signs of prior handling and storage, as pictured. Review the supplied photographs for the unit's visible condition and included components.
Shipping & Receiving
- Professionally packaged for transport
- Inspect the shipment promptly upon arrival
- Report shipping damage promptly
- Follow the receiving facility's equipment intake and evaluation procedures before placement into service
Return Eligibility
See the product page and store Return & Refund Policy for the applicable return period and eligibility requirements.
Technical Details
| Brand | Agilent Technologies |
|---|---|
| Category | Helium Leak Detector |
| Medical Discipline | Laboratory |
| OEM | Agilent Technologies |
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.
