alveoMD®

We would like to inform our valued users that our application is currently available on Android devices. However, it is not available for iOS devices at this time. We are committed to providing a high-quality experience and are considering expanding our platform availability in the future. Stay tuned for updates and thank you for your understanding.

The alveofit®/alveoMD® application is designed to work with Android devices running version 8.0 (Oreo) or higher.
Checking Your Android Version: Users can check their Android version by going to Settings > About Phone > Software Information on their device. If your version is below 8.0, an update may be required to use alveofit®/alveoMD®. Note: Users with devices running Android versions older than 8.0 may not be able to install or run the alveofit®/alveoMD® app effectively. We encourage users to consider updating their device software or using a compatible device to access all the features of alveofit®/alveoMD®.

Thank you for your understanding and we look forward to offering you a seamless experience on alveofit®/alveoMD®.

Certainly! Here’s an elaborated FAQ entry explaining how the alveoair device supports the Chrome-based AlveoConnect Portal:

FAQ: alveoair Device Support for Chrome-Based alveoConnect® Portal

Q: Does the alveoair device support the Chrome-based alveoConnect® Portal?

Ans: Yes, the alveoair device is fully compatible with the alveoConnect® Portal when accessed via the Google Chrome browser. Below are key points that elaborate on this compatibility:

Chrome Optimization: The alveoConnect® Portal is optimized for Google Chrome, ensuring a smooth and efficient user experience. This means when you access the portal using Chrome, you can expect enhanced functionality, speedy performance, and a user-friendly interface.

Device Integration: alveoair devices seamlessly integrate with the alveoConnect® Portal via Chrome. This integration allows users to access real-time data, manage device settings, and utilize various features available on the portal.

Cross-Platform Accessibility: Chrome’s cross-platform nature allows users to access the alveoConnect® Portal from various devices, including desktops, laptops, and tablets, provided they are using the Chrome browser. This ensures consistent access and experience regardless of the device used.

Why Chrome: Google Chrome is known for its robust security features, fast performance, and frequent updates. These attributes make it an ideal choice for accessing web-based platforms like the alveoConnect® Portal, ensuring data is transmitted securely and efficiently.

How to Access: To access the alveoConnect® Portal, users should navigate to the portal’s URL using the Chrome browser. Once logged in, the portal will automatically detect and sync with the alveoair device, allowing for real-time monitoring and management.

Technical Requirements: Users should ensure their Chrome browser is up to date to take full advantage of all the features and security updates. The alveoConnect® Portal is designed to work with the latest versions of Chrome for optimal performance.

Support and Assistance: If users encounter any issues while using the alveoConnect® Portal with their alveoair device on Chrome, they are encouraged to contact our support team for assistance.

Note:– While the alveoConnect® Portal is optimized for Chrome, it may also be accessible through other browsers. However, for the best experience and full functionality, we highly recommend using Google Chrome.

We are committed to providing a seamless and efficient experience for all our users through the alveoair device and the alveoConnect® Portal.

If the alveoair device is kept mostly in idle mode, which means it is turned on but not actively used for testing, it can last up to 7 years.

Idle mode consumption is significantly lower, as the device is not actively engaging its sensors and processing capabilities to the same extent as during active testing.

Factors Influencing Longevity:

Battery Life: Regular use tends to consume more battery, reducing the overall lifespan of the device.

Wear and Tear: Regular testing may also contribute to general wear and tear of the components, affecting longevity.

Storage Conditions: How the device is stored, particularly when in idle mode, can impact its lifespan. Ideal storage conditions can prolong the life of the device.

Maximizing Device Longevity:

To maximize the lifespan of your alveoair device, it is recommended to follow the manufacturer’s guidelines for use and storage.

Regular maintenance and firmware updates, if available, can also help in ensuring the device functions optimally for the longest possible time.

Replacement and Upgrades:

Considering technological advancements and potential wear over time, users may consider replacing or upgrading their alveoair device at the end of its estimated lifespan for optimal performance and access to the latest features.

Note:- These estimates are based on average usage scenarios. Actual device longevity can vary based on individual usage patterns, environmental conditions, and adherence to maintenance guidelines.

The alveoair device is designed with durability in mind, ensuring reliable performance throughout its estimated lifespan under the given usage conditions.

Creating a detailed guideline for performing spirometry with the alveoair device involves several steps to ensure accurate and safe testing. Please note that this is a general guide and it’s important to always refer to the specific instructions provided with your alveoair device. Here’s a basic outline:

Guideline for Performing Spirometry with alveoair

Preparation:

Read the Manual: Before using the alveoair spirometer, thoroughly read the user manual. Understand the device’s features, limitations, and safety precautions.

Charge the Device: AAA Batteries should be charged or have adequate battery life for the test.

Hygienic Practices: Clean and sanitize the device according to the manufacturer’s instructions to prevent any risk of infection.

Setting Up:

Install Necessary Software/App: If the alveoair requires specific software or an app for operation, ensure it is installed and updated on your compatible device (smartphone, tablet, or computer).

Device Connection: Connect the alveoair spirometer to your device. This might be done via Bluetooth, Wi-Fi, or a physical connection, depending on the model.

Patient Information: Enter the patient’s details into the system as required. This may include age, gender, height, weight, and medical history relevant to the spirometry test.

Performing the Test:

Patient Position: Have the patient sit upright, in a comfortable position. Ensure they are relaxed and their airway is not obstructed by clothing.

Instructions: Clearly instruct the patient on how to perform the test. They will need to take a deep breath in, then exhale forcefully and as completely as possible into the spirometer.

Mouthpiece Use: The patient should seal their lips tightly around the mouthpiece. Stress the importance of a tight seal to prevent air from escaping.

Perform Multiple Tests: Usually, multiple tests (e.g., three trials) are performed to ensure consistency and accuracy. Wait for about 30 seconds to one minute between tests to allow the patient to recover.

After the Test:

Review Results: The software or app will likely provide immediate results. Review these for any irregularities or the need for repeat tests.

Clean the Device: After testing, clean and sanitize the device according to the manufacturer’s guidelines.

Consult Healthcare Professional: If the test is self-administered, it’s recommended to share and discuss the results with a healthcare professional for accurate interpretation.

Safety and Precautions:

Patients with certain health conditions (like recent heart surgery, eye surgery, active lung infections, etc.) should consult with a healthcare professional before performing spirometry.

If the patient feels dizzy, lightheaded, or experiences chest pain during the test, stop immediately and seek medical advice.

Note:- This guideline is for general informational purposes. Always follow the specific instructions provided with your alveoair device and consult healthcare professionals for medical advice.

Remember, spirometry tests are sensitive to technique and patient effort, so proper instruction and practice are key to obtaining reliable results.

Certainly! Here’s an overview of the contents found in the alveoair Spirometer box:

Contents of the alveoair Spirometer Box

When you purchase the alveoair Spirometer, the box will contain the following items:

alveoair Spirometer Device:

Quantity: 1

Description: This is the main unit of the alveoair Spirometer, the device used for conducting spirometry tests. It’s designed to measure lung function and airflow.

Batteries:

Quantity: 2 AAA batteries

Description: These are used to power the alveoair Spirometer. Ensure that these batteries are inserted correctly for the device to function.

Turbine:

Quantity: 1

Description: The turbine is a crucial component of the spirometer. It’s used to measure the flow rate of air entering and exiting the lungs during the spirometry test.

Additional Information:

Along with these primary components, the box may also include a user manual or guide. This manual provides important information on how to use the device, safety instructions, and maintenance guidelines.

It’s advisable to read the user manual thoroughly before using the device.

Some models might include additional accessories like disposable mouthpieces, nose clips, or carrying cases, depending on the manufacturer’s package.

Note:- Always check the contents upon receiving your alveoair Spirometer to ensure all items are present and in good condition. If anything is missing or damaged, contact the supplier or manufacturer immediately for assistance.

This overview gives you a clear idea of what to expect in the alveoair Spirometer box, ensuring you are well-prepared for its use.

You can connect with support@alveo.fit for details to extend the warranty

Thank you for the clarification. Based on your information:

Yes, the alveoair Spirometer is FDA-approved with 510(k) clearance.**

The 510(k) clearance from the United States Food and Drug Administration (USFDA) indicates that the alveoair Spirometer has been reviewed and found to be substantially equivalent to another legally marketed device. This clearance is a significant milestone, ensuring that the device meets strict standards for safety and effectiveness set by the FDA.

What This Means:

Safety and Effectiveness: The 510(k) clearance affirms that the alveoair Spirometer is safe and effective for its intended use.

Regulatory Compliance: This approval also means that the device complies with regulatory requirements for medical devices in the United States.

Quality Assurance: Users and healthcare professionals can have confidence in the quality and reliability of the alveoair Spirometer.

For Users:

If you’re considering using the alveoair Spirometer, this FDA approval provides assurance of its quality and safety standards, making it a trustworthy choice for spirometry testing.

It’s always recommended to check the latest documentation provided with the device for any updates or changes in its regulatory status.

Certainly! Here’s a detailed answer for signing in to the alveofit®/alveoMD® application:

How to Sign In to alveofit®/alveoMD®

To sign in to the alveofit®/alveoMD® application, follow these steps:

Download the Application:

Firstly, download the alveofit®/alveoMD® application from the Google Play Store if you are using an Android device. Ensure your device is running Android version 8.0 or higher, as this is the minimum requirement for the app.

Open the Application:

Once the application is downloaded, open it on your device.

Registration (For New Users):

If you are a new user, you will need to register first. Look for an option typically labeled ‘Register’.

During registration, you will be asked to provide information such as your name, email address, and other relevant details. You will also create a username and password. Ensure you choose a secure password.

After filling in the required information, follow the prompts to complete the registration process. This may include verifying your email address or phone number.

Sign In (For Existing Users):

If you already have an alveofit®/alveoMD® account, select the ‘Sign In’ option.

Enter your username and password that you created during the registration process.

If you’ve forgotten your password, look for a ‘Forgot Password’ link to reset it.

Accessing the Application:

After successfully signing in, you will have access to the features and functionalities of the alveofit®/alveoMD® application.

Note: It’s important to keep your login credentials secure and not share them with others. If you encounter any issues during the sign-in process or have any questions, you can usually find a ‘Help’ or ‘Support’ option within the app or on the alveofit®/alveoMD® website.

By following these steps, you should be able to easily sign in to the alveofit®/alveoMD® application and access its features. Remember, if you are a new user, registration is a necessary first step.

For detailed assistance or inquiries, please feel free to reach out to our Support team by sending an email to support@alveo.fit. They are ready to help you with any questions, concerns, or actions you may need.

No, the alveoMD® application does not retain any data once the account is deleted.

No, the alveoMD® application does not retain any data once the account is deleted.

The alveoair device is covered by a one-year warranty, subject to specific conditions. The warranty stipulates that the device should not have water damage or physical breakage for the coverage to be valid. If the device experiences defects in materials or workmanship during the warranty period and has not been subjected to water damage or physical breakage, the manufacturer typically commits to repairing or replacing the device, or providing necessary parts or service at no additional cost to the user. It’s crucial to thoroughly review the terms and conditions of the warranty for a comprehensive understanding of the coverage, limitations, and any actions required on the user’s part to maintain warranty validity.

To reset your password, follow these steps based on your login status:

If Already Logged In:

Navigate to the Profile Screen.

Select “Change Password” to reset your password.

If Not Logged In:

Click on “Forgot Password.”

Verify your Username using the Reset Code sent to your registered Mobile/EmailId.

For an already logged-in session, use the Profile Screen to change the password. If not logged in, initiate a password reset via “Forgot Password,” completing the process by verifying your Username through the Reset Code sent to your registered mobile or email.

Predicted values in a Spirometry test are determined based on individual demographic details such as height, weight, race, age, and gender. These values serve as a benchmark for assessing an individual’s lung function, allowing comparison with actual test results. Predicated values help identify how well a person’s lung function aligns with expected norms, considering their specific characteristics. This comparison aids in evaluating respiratory health and potential deviations from the anticipated lung function for a given demographic profile.

Interpreting spirometry results involves analyzing various parameters to assess lung function. Here are key components and considerations in interpreting spirometry results:

Forced Expiratory Volume in 1 second (FEV1):

Normal: A healthy individual usually has an FEV1 that is around 80-120% of the predicted value.

Obstructive Lung Disease: A reduced FEV1 suggests difficulty in expelling air quickly, common in conditions like asthma or chronic obstructive pulmonary disease (COPD).

Forced Vital Capacity (FVC):

Normal: FVC should be within the predicted range for a healthy individual.

Restrictive Lung Disease: Reduced FVC may indicate restrictive lung diseases, where the lung expansion is limited, such as pulmonary fibrosis.

FEV1/FVC Ratio:

Normal: A normal ratio is typically around 70-80%.

Obstructive Lung Disease: A lower FEV1/FVC ratio (less than 70%) suggests airway obstruction, common in conditions like COPD.

Peak Expiratory Flow (PEF):

Normal: PEF varies based on age, sex, and other factors.

Obstructive Lung Disease: Reduced PEF may indicate airway narrowing or obstruction.

Interpretation Based on Patterns:

Obstructive Pattern: Reduced FEV1 and FEV1/FVC ratio, typical in asthma or COPD.

Restrictive Pattern: Reduced FVC with a normal or increased FEV1/FVC ratio, common in conditions limiting lung expansion.

Comparison with Predicted Values:

Results are compared with predicted values based on demographic factors (age, gender, height, etc.).

Deviations from predicted values help identify abnormalities or diseases.

Interpretation is complex and should consider the patient’s medical history, symptoms, and other diagnostic tests. Consulting with a healthcare professional, typically a pulmonologist or respiratory therapist, is crucial for a comprehensive understanding and accurate diagnosis.

Yes, we have an open API that facilitates integration with third-party applications or institutions. Our application supports fast healthcare Interoperability Resources (FHIR) APIs for seamless integration. Additionally, we offer Software Development Kits (SDKs) specifically designed for android application integration. These tools provide flexibility and compatibility for a smoother integration experience with external systems. For detailed information or assistance with the integration process, please contact our support team support@alveo.fit.

Certainly. The alveoair device features clear indicators for its wireless connection with the alveoMD® application. Users can observe LED light blinks on the device, and on the alveoMD® application screen, there are visual cues confirming the successful connection. These indicators serve to easily communicate the device’s connectivity status to the user.

No, each alveoair device is associated with a single user. However, the alveoMD® application can be installed on multiple mobile devices, allowing the same user to perform tests using different devices.

The alveoair device supports AAA batteries.

Certainly, You can generate a PDF report of your spirometry test within the alveoMD® application. After generating the report, you can view it using a PDF viewer and share it via email, WhatsApp, or other sharing options as needed.

The warranty period for the alveoair device commences from the date of device registration and extends for a duration of one year. During this period, users are entitled to warranty coverage, which typically includes repair or replacement of the device for eligible issues. It is crucial for users to carefully review the terms and conditions specified in the warranty policy, as well as any requirements or limitations outlined by the manufacturer. For comprehensive details regarding warranty coverage, initiation, and any potential extensions, users should refer to the official documentation provided by the manufacturer or contact the customer support team for accurate and up-to-date information.

Certainly, your health information on the alveoMD® app is secure. We adhere to HIPAA compliance standards, ensuring the confidentiality and protection of all personal and health-related data.

If you encounter a technical issue with the app, please reach out to our support team for assistance. You can connect with us by emailing support@alveo.fit. Our support team is ready to provide guidance, troubleshoot any issues, and ensure a smooth experience with the application. Feel free to describe the problem you’re facing in your email for a more efficient resolution.

Spirometry, a common pulmonary function test, is generally safe; however, there are certain contraindications and considerations to be aware of. Contraindications may include:

Recent Surgery: Individuals who have had recent eye, chest, or abdominal surgery may be advised against spirometry due to concerns about increased pressure during forced exhalation.

Cardiac Issues: Severe cardiovascular conditions, such as a recent heart attack or unstable angina, may be contraindications.

Respiratory Infections: Active respiratory infections, like pneumonia or bronchitis, may interfere with the accuracy of spirometry results.

Recent Eye Surgery: Some eye surgeries, such as laser surgery, can be contraindications due to the increased intraocular pressure during forced exhalation.

Uncontrolled Hypertension: Extremely high blood pressure that is not well-controlled may pose risks during spirometry.

Physical Limitations: Individuals with physical limitations preventing them from performing the necessary maneuvers for the test may find spirometry challenging.

It is crucial for healthcare professionals to consider a patient’s medical history, current health status, and any potential contraindications before performing spirometry. If there are concerns or contraindications, alternative diagnostic tests or modified procedures may be considered. Always consult with a qualified healthcare provider for personalized advice based on individual health conditions.

Users can stay updated with the latest features and improvements by checking the Google Play Store. For the most recent version of the alveoMD® application, please refer to the following download URL: alveoMD® on Google Play Store.

Users should verify the correctness of their username and password. If experiencing difficulty, they can use the “Forgot Username” or “Forgot Password” options to retrieve or reset their credentials.

Race is one of the demographic factors that might be considered in the interpretation of spirometry test results. It is not inherently required for the test itself, but including demographic information such as race in the interpretation can be relevant for establishing reference values.

In spirometry, reference values are often based on large population studies, and they can vary among different racial and ethnic groups. Including demographic information allows for a more accurate interpretation of an individual’s lung function by comparing their results to a reference population that shares similar characteristics, including race.

It’s important to note that the use of race in medical measurements and research is a complex and debated topic. While it may contribute to more accurate interpretations of lung function for certain populations, it is not the sole factor, and healthcare providers consider a range of factors to assess an individual’s respiratory health accurately.

Always consult with healthcare professionals to understand why specific demographic information, such as race, is being collected and how it may impact the interpretation of medical tests. Privacy and ethical considerations are also crucial in handling such demographic data in a healthcare setting.