【EXPERT Q&A】What is the difference between medical devices and non-medical devices?

September 27, 2024  Source: drugdu 32

Drugdu.com expert's response:

 

The differences between medical devices and non-medical devices are primarily manifested in the following six aspects:

Ⅰ. Definition and Purpose

Medical Devices: Refer to instruments, equipment, appliances, in vitro diagnostic reagents and calibrators, materials, and other similar or related articles, including the necessary computer software, that are directly or indirectly used on the human body. Their efficacy is primarily obtained through physical means rather than through pharmacology, immunology, or metabolism, or if these means are involved, they only play an auxiliary role. The primary purposes include diagnosis, prevention, monitoring, treatment, or alleviation of diseases, as well as diagnosis, monitoring, treatment, alleviation, or functional compensation of injuries.

Non-Medical Devices: Generally refer to products that are not directly used on the human body or, even if in contact with the human body, do not have a medical purpose. They may be daily necessities, industrial products, consumer goods, such as fitness equipment, beauty products, ordinary glasses, household items, etc.

Ⅱ. Regulatory Requirements

Medical Devices: Are strictly regulated by national medical product administration departments and must undergo a registration and approval process before being marketed and sold. Manufacturers must comply with relevant regulations and standards, such as the Medical Device Supervision and Administration Regulations. The design and production processes must follow a more rigorous quality management system, such as ISO 13485.

Non-Medical Devices: May be regulated by different departments depending on their nature and intended use, but the regulatory requirements are generally not as stringent as those for medical devices.

III. Safety and Effectiveness

Medical Devices: Must undergo rigorous safety and effectiveness evaluations to ensure that they will not harm the human body during use. The evaluation process includes clinical evaluations and testing to ensure the safety and effectiveness of the product.

Non-Medical Devices: While also requiring user safety, they typically do not undergo the same level of clinical evaluations and testing as medical devices.

Ⅳ. Labeling and Instructions

Medical Devices: Must have clear labeling, including the medical device registration number, date of manufacture, expiration date, instructions for use, etc. These labels and instructions are crucial for ensuring the correct use and safety of the product.

Non-Medical Devices: Also require labeling and instructions, but the content may focus more on product ingredients, usage methods, and maintenance.

Ⅴ. Scope of Use and Target Population

Medical Devices: Have specific functions and intended users. They should not be used outside their intended scope and must be used strictly according to the applicable scope stated in the product registration certificate and instructions for use.

Non-Medical Devices: Have a broader scope of application, and their primary functions are not specifically medical but rather related to the individual efficacy of the product.

Ⅵ. Design Philosophy and Process

Medical Devices: The design philosophy places greater emphasis on the auxiliary effects and functions of the product. The design process must include all design materials, and the design process itself is necessary, as no approval will be granted without it. Additionally, considerations must be given to factors such as product lifespan, durability, and consumable design.

Non-Medical Devices: The design philosophy prioritizes ease of use and user preference. The design process is relatively conventional and does not have many unique features.

In conclusion, medical devices and non-medical devices exhibit distinct differences in definition, purpose, regulatory requirements, safety and effectiveness, labeling and instructions, scope of use and target population, as well as design philosophy and process. These differences underscore the uniqueness and importance of medical devices as specialized products.

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By editor
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