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RESPIRATORY TRAINER MARKET ANALYSIS

Respiratory Trainer Market, by Product Type (Resistance Training Devices and Endurance Training Devices), by Technique (Inspiratory Muscle Training, Expiratory Muscle Training, and Combination of Both), by Disease Indication (Asthma, Chronic Obstructive Pulmonary Disease, and Others), by End User (Children and Adults), and by Region (North America, Europe, Asia Pacific, Middle East, Africa, and Latin America) - Size, Share, Outlook, and Opportunity Analysis, 2022 - 2030

  • Published In : Jun 2022
  • Code : CMI3336
  • Pages :191
  • Formats :
      Excel and PDF
  • Industry : Medical Devices

Market Challenges And Opportunities

Global Respiratory Trainer Market: Restraint

Product recall and critical regulatory compliance procedures may act as a restraint for growth of the respiratory trainer market. For instance, in July 2021, the U.S. Food and Drug Administration (FDA) directed Philips Respironics, a medical devices company to recall millions of sleep and respiratory devices following concerns that foam in the devices, which is used to reduce sound and vibration, may break into particles and enter the air hose of the device and be inhaled by the user.

Moreover, in 2020, the U.S. FDA issued guidance to formulate a policy to help expand the availability of ventilators as well as other respiratory devices and their accessories during the COVID-19 pandemic.  

Market Drivers

  • Rising incidence of respiratory disorders
  • Increasing respiratory trainer device launches and approvals

Product recall and critical regulatory compliance procedures may act as a restraint for growth of the respiratory trainer market. For instance, in July 2021, the U.S. Food and Drug Administration (FDA) directed Philips Respironics, a medical devices company to recall millions of sleep and respiratory devices following concerns that foam in the devices, which is used to reduce sound and vibration, may break into particles and enter the air hose of the device and be inhaled by the user.

Moreover, in 2020, the U.S. FDA issued guidance to formulate a policy to help expand the availability of ventilators as well as other respiratory devices and their accessories during the COVID-19 pandemic.  

Restraints

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