Powers On
YesCosmetic
GoodCosmetic Condition
New in box
Excellent
Good
Poor
Overview
Description:
The GN Otometrics Madsen Astera Clinical Audiometer Ref 8-04-13102 is an audiometric testing instrument designed for use in compatible audiology and clinical environments. Its electronic testing platform provides an interface for conducting hearing assessment procedures using compatible accessories and equipment configurations. The Madsen Astera features a clinical audiometer design intended for integration into professional audiology workstations and hearing assessment setups.
Specifications:
Brand: GN Otometrics
Product Line: Madsen
Model: Astera
Reference Number: 8-04-13102
Product Type: Clinical Audiometer
Equipment Type: Audiometric Testing Equipment
Function: Audiometric Testing and Hearing Assessment
Application: Audiology / Clinical Environments
Features:
Madsen Astera clinical audiometer design
Electronic audiometric testing platform
Designed for compatible audiology accessories
Clinical equipment configuration
Suitable for professional audiology environments
Technical Details
| Brand | GN Otometrics |
|---|---|
| Category | Clinical Audiometer |
| Medical Discipline | Internal Medicine |
| Condition | Used |
| Cosmetic Condition | Good |
| Powers On | Yes |
| OEM | GN Otometrics |
| SKU | DA42-ITEM-U - P |
| 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.
