Withan intuitive user interface, handheld design and easy data export functionality, The MIR MiniSpir Light Spirometer can optimize your workflow with ease. This spirometer also features an Embedded Temperature Sensor for BTPS Conversion as well as Turbine Calibration for maximum accuracy.
The MIR MiniSpir Light Spirometer measures the essential parameters for diagnostic spirometry and is ideal for Occupational, Sport and Pediatric Medicine. Additionally, the MiniSpir Light comes standard with a light version of the WinspiroPRO high-performance PC spirometer software for dynamic data management.
The light version of the WinspiroPRO Software comes standard with the MIR Minispir Light. This software allows all patient records to be displayed on single-screen patient cards with dynamic data management. Additionally, the data can be sent to a database in an EMR, hospital or occupational health system. For more information, click here.
The MIR MiniSpir Light measures less parameters than the MIR MiniSpir and does not have optional capacilities for Pulse-Oximetry, 6MWT, Sleep Test, SPO2 and BPM Spot Check. Additionally, the MiniSpir Light Spirometer does not use Reusable Turbines and is only compatible with the Light version of the WinspiroPRO Software.
From time to time, Best Practice will release new versions of Bp Premier, the latest being BP Orchid SP1 (1.12.1.x) and soon to be BP Orchid SP2 (1.12.2.x). These updates tend to include changes to the Best Practice device interface and will likely cause old integration software to fail connecting to Bp Premier. When attempting to start a test, an error message will be displayed.
LEMR provides integration with many devices, and is continually developed to maintain compatibility with new editions of Best Practice software. To get your devices up and running again with ongoing support, contact us!
LEMR version 2023.9.26.1105 and newer are compatible with Bp Premier Orchid and maintains backwards compatibility with older versions of Bp Premier. If you already have LEMR and need an update, please contact us.
A procedure to check that everything is working correctly is required before you start testing. The OSHA standard on this subject does not enforce you to use an electro-acoustic ear simulator, but states that a daily check should be performed to ensure the audiometer is working correctly. You could use an electro-acoustic ear simulator or a known hearing level such as your own hearing level as part of this.
The values shown in the following document relate to the Interacoustics DD45 supra-aural audiometric earphones with pure tone. These values have been measured by the accredited national laboratories PTB in Germany and DTU in Denmark according to studies commissioned by the William Demant Diagnostics Group.
Prior to delivery, your audiometer is calibrated to a specific pair of headsets. It is essential the headsets are used only with this audiometer and channel (ear) to which they are calibrated. However, you can change the headset lead without affecting the calibration of your audiometer. Before you start, please note here the audiometer and headset details for reference:
When replacing the probe tip, ensure that the seal is correctly inserted with its flat edge aligned with the flat edge on the probe tip. Push the probe tip over the boss and replace the nose cone. Make sure that the nose cone is screwed home firmly but do not over-tighten. Do not use any tools to tighten the nose cone.
Winspiro PRO has historically been included with the Spirolab and Spirodoc; located with the spirometer on a USB stick. Registration of the Spirolab and Spirodoc software (Winspiro PRO) is now done by the user.
Winspiro PRO now comes with lifetime upgrades at no charge, so you will always be running the latest version. A network version is available upon request. To view a demonstration of the Winspiro PRO installation process, click here.
To register Winspiro PRO software, you need to create an account with MIR. This can be done via the MIR website. This will provide access to MIR support features, enhanced tools, resources and updates on your MIR products and software.
You could be running two types of tympanometry software. This will either be Amplivox Amplisuite or the NOAH impendence module. The minimum specification for NOAH4 can be found on the HIMSA website. The Amplisuite specifications are:
Should be thoroughly cleaned in between each patient encounter. All surfaces internally and externally should be wiped down with an acceptable disinfectant. Equipment should be cleaned as per your existing infection control procedures.
Typically, these booths have a small fan built into the roof to draw air from the host space. The air in the host room is thus the deciding factor, assuming this is properly addressed we would recommend leaving the booth door open between patients.
Larger booths might well be connected to a main ventilation system that serves parts of the Hospital. In this case we would recommend leaving the booth empty with the door closed for at least 10 minutes between each patient to allow for one full cycle of air exchange.
Please do not attempt to steam clean the fabric lining, we would instead advise that patients are discouraged from touching the walls. If a patient were to touch the walls, we would recommend they wash their hands or sanitize with gel. Fabric walls can be sprayed with disinfectant, but this should be done from a distance to avoid soaking the lining. All hard surfaces should be wiped down as above.
VALIDATED LIST: 70% isopropyl alcohol / Bactynil Disinfectant Wipes / Clorox Healthcare Bleach / Super Sani Cloth / Mikrozid AF wipes / Mikrozid Universal wipes premium recommendations (application times).
Clean the instrument by wiping the outer case with a lint free cloth lightly dampened with cleaning solution. Recommended cleaning and disinfection solutions are warm water with mild, non-abrasive cleaning solution (soap) and/or clinical wipes (e.g. Clinell Universal).
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Objective: The current research study aimed to access the relationship between obesity and asthma exacerbations and severity among adult patients at the outpatient section of a federal hospital (PIMS) in Islamabad, Pakistan.
Methods: A cross-sectional research study was carried out on 207 asthma adult patients belonging to different areas and ethnic groups from the country. The study setting was the PIMS hospital, which attracts patients from all over the country due to its facilities and cost-effective treatments. The body mass index (BMI) of asthma patients was calculated using the heights and weights of the study subjects. However, the pulmonary functions were calculated using a computerized spirometer i-e Spirolab III S/N 303681 in line with Winspiro PRO 7.1.version software. It presents the patient's forced vital capacity that expires in the first second of expiration to full (FEV1) in comparison to forced vital capacity (FVC) ratio, that is, Tiffeneau-Pinelli index was also recorded to determine the asthma severity.
Conclusion: The study subjects presented raised asthma severity in accordance with the raised BMI. Obese patients presented comparatively raised asthma exacerbations. Moreover, a statistically significant association of gender difference was observed between obesity and asthma severity. It was concluded that adult asthmatic women with obesity presented raised asthma severity as compared to adult asthmatic males.
The displayed information indicates the present stock level of this item. Additional quantity is available and may have an extended estimated delivery range. We will provide you with regular updates throughout the order process.
This item will be shipped directly from the manufacturer to your doorstep, ensuring that you receive the newest product available. The estimated delivery range provided is based on the manufacturer's inventory levels and is subject to change depending on the quantity ordered. We ship items as soon as they become available, so if you order multiple quantities, you may receive them in separate shipments.
A special order item will need to ship to our warehouse from the manufacturer before then shipping to you. The estimated delivery range that you see is based on the information that we receive from the manufacturer, which is also contingent upon your ordered quantity and the current inventory levels of the manufacturer. We will ship the items to you as soon as they become available, which may result in multiple shipments if you order more than one quantity.
The The MIR Spirolab Spirometer with Oximeter configuration includes PC software, a USB cable, a miniflowmeter with cable, an adult reusable Oximetry sensor, a power supply/battery charger, one roll of thermal paper, a nose clip, a carrying case, and a user manual.
This software contains curves and tests in various formats including Word, Excel, Adobe Acrobat, HTML, and text file. WinspiroPRO is compatible with Windows XP, Vista, 7, 8, and 10. WinspiroPRO drivers have been certified by Microsoft. Network version available, and WinspiroPRO is now available with HL7 interface.
We strive to offer excellent customer service at MFI Medical, which is why we offer all our customers access to dedicated account managers. Our team of knowledgeable account managers is committed to helping you find the perfect product at the best available price. You can rely on them for guidance and support whenever you need it.
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