Microsite Template for Medical Device Manufacturers

What Goes Into Naming a Healthcare Product? A name that tells a story tells doctors and patients something about the device/drug. A name that indicates how the product works and can be inspired not only by what the device/drug does but the mechanism by which is does it.

The Global Medical Device Nomenclature (GMDN) provides a generic system to identify medical device products used to diagnose, monitor, treat and prevent disease or injury. It provides a generic or common name for devices. The system allows sharing of data on medical device use, supporting patient safety.

Set yourself up for success by getting to know the ins and outs of starting a medical supply business. Choose a medical niche or underserved market. Determine your business type. Beneficial ownership information reporting. Secure your operating licenses. Fund your business. Identify vendors and distributors.

Class III devices are high-risk devices that are very important to health or sustaining life. Examples include pacemakers and deep-brain stimulators.

The Universal Medical Device Nomenclature System (UMDNS) is a standard worldwide nomenclature for medical devices that has been officially adopted by many nations. It is produced by the ECRI Institute. Purpose. UMDNS is a standard international nomenclature and computer coding system for medical devices.

Medical devices vary in both their intended use and indications for use. Examples range from simple, low-risk devices such as tongue depressors, medical thermometers, disposable gloves, and bedpans to complex, high-risk devices that are implanted and sustain life.

What is nomenclature for medical devices? The nomenclature of medical devices is a coding and naming system used to generically classify and identify all medical devices and related health products.

The MHRA 2023 defines a medical device as any instrument, apparatus, appliance, material software or other article that may be used on a patient for the purposes of: Diagnosis, prevention, monitoring, treatment or alleviation of disease. Diagnosis, monitoring, treatment, alleviation of, or compensation for, an injury.

ISO 13485 is designed to be used by organizations involved in the design, production, installation and servicing of medical devices and related services. It can also be used by internal and external parties, such as certification bodies, to help them with their auditing processes.

Medical devices range from simple tongue depressors and bedpans to complex programmable pacemakers, and closed loop artificial pancreas systems. Additionally, medical devices include in vitro diagnostic (IVD) products, such as reagents, test kits, and blood glucose meters.