Secondhand Fisher-Paykel MyAirvo 2 High Flow Device

Objective AI Report

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Report date: 26.11.2025

Fisher & Paykel MyAIRVO 2 High Flow Therapy Device Analysis Report

Device Detection and Identification

The main device examined in the visuals is a humidifier system with an integrated flow generator, used to provide respiratory support in home care and clinical settings. The device consists of a main unit standing upright with an LCD screen and control buttons, a transparent water chamber integrated into its front, and a heated breathing circuit connected to the device.

Brand and Model

As a result of a detailed examination of the device’s front panel and accompanying documents, the following brand and model information has been definitively identified:

• Brand: Fisher & Paykel
• Model: MyAIRVO 2

The logo on the product clearly reads “Fisher & Paykel HEALTHCARE myAIRVO 2”. Additionally, original model-specific part codes such as “900PT422 Oxygen Inlet Kit” and “HC360” (humidifier chamber user manual code) are present on the accessory packages.

Areas of Use

The MyAIRVO 2 is designed to provide heated and humidified high-flow air/oxygen mixtures to spontaneously breathing patients. It is commonly used in chronic respiratory conditions such as COPD or in tracheostomized patients to keep airways moist and support mucociliary clearance.

Accessories and Package Contents

The visuals show a rich set of accessories supplied with the device. The identified parts are:

• 1 Fisher & Paykel MyAIRVO 2 Main Unit.
• 1 MR290 (or compatible model) Auto-filling Humidification Chamber (attached to the device).
• 1 AirSpiral Heated Breathing Tube/Circuit (attached to the device, spiral-structured).
• 1 Original Black Carrying Bag (with strap, perfectly fitting the device dimensions).
• 1 Oxygen Inlet Kit (package reads “2/myAIRVO 2 Oxygen Inlet Kit 900PT422”).
• 1 Pack of Spare Air Filters (white rectangular filters in a clear pouch).
• 1 User Manual (HC360 and device image on the cover).
• 1 Quick Start Guide / Brochure (F&P myAIRVO 2 titled, spiral/laminated card).
• Weekly change reminder labels (yellow strips, with text like “Change on Monday”, etc.).
• Patient Interfaces: Cannula/mask sets are visible in clear packaging inside the bag. One package reads “Duet”, and another package shows “Kid” and “yMask” indicating pediatric compatibility.

Quantity Information

The visual shows 1 main device and the necessary consumables/accessories (tube, chambers, filters, kits, bag, and documents) for its operation, all as a collective set.

Visual and Cosmetic Condition

The cosmetic condition of the device has been visually assessed as excellent. No yellowing, cracks, deep scratches, or impact marks were found on the white plastic casing of the main unit. The blue parts retain their vibrancy. The overall appearance of the device suggests it has been used very little or meticulously maintained.

Mechanical and Physical Checks

• Water Chamber: The humidification chamber attached to the front of the device appears transparent and clean. No significant calcification, residue, or clouding was observed inside, indicating little use or good cleaning.
• Tube Connection: The heated circuit tube is properly connected to the device. No crushing, tearing, or bending deformation is visible on the tube. The orange label/protector is present at the tube’s connection point to the device.
• Buttons: The four control buttons on the front panel (Power, Up, Down, Mode) are intact and in place. The symbols on the buttons are not erased.
• Bag: The carrying bag is fabric, with no visible fraying or stains. Zippers and strap attachments appear sturdy.

Electronic Components and Screen Analysis

The device is in the off position in the visuals (screen is black). Therefore, no visual comment can be made regarding pixel errors or screen backlighting. However, there are no scratches or cracks on the screen surface. No external findings that would compromise the electronic integrity of the device (e.g., water contact marks, rust) were encountered.

Documents and Label Information

The presence of original user manuals and “HC360” coded technical brochures with the product is positive for tracking the device’s history and ensuring correct use. Furthermore, the label on the “Oxygen Inlet Kit” confirms the part’s reference number is 900PT422. The weekly reminders on the yellow labels indicate their use for hygiene tracking.

General Condition and Potential Risk Analysis

Based on the available visuals, despite being second-hand, the product can be categorized as “near new” or “very clean”. The clarity of the water chamber and the fact that some accessories (filters, oxygen kit, cannula) are in sealed packaging indicate that the device is in good hygienic condition. As no visible physical damage (breakage, cracks, oxidation) was found, no potential malfunction risk is foreseen based on the visuals.