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Health care in Poland is provided through the Narodowy Fundusz Zdrowia, a publicly supported health care system, and is free for all Polish citizens as long as they qualify as “insured.” Everyone in Poland has a constitutional right to seek health care, as stated in Article 68 of the Polish Constitution.
Equal access to the publicly funded healthcare system is provided to all citizens. The government is required to offer free health care in particular to infants, expectant mothers, people with disabilities, and the elderly. Poland, meanwhile, makes heavy use of private healthcare. Uninsured patients are responsible for the full cost of all medical services.
Any device intended by the manufacturer to be used, either alone or in combination, for a medical purpose qualifies as a medical device. This includes instruments, apparatuses, implements, machines, appliances, implants, reagents for in vitro use, software, materials, and other similar or related items.
The Poland Medical Devices Market accounted for $XX Billion in 2023 and is anticipated to reach $XX Billion by 2030, registering a CAGR of XX% from 2024 to 2030.
ADYTON Inc. is a privately held business with its corporate headquarters in Prague, the centre of the European Union, with subsidiaries in Slovakia and Poland.
Currently, the business is one of the leading suppliers of medical technology goods. They collaborate with manufacturers that are among the leading technological firms in the world to make their medical products and healthcare solutions available to more than 53 million people in their region.
With the most up-to-date, well-proven medical technology, they are providing treatments for serious health disorders that improve people’s quality of life. Their primary concern is the calibre of the goods and services they provide. As a result, the business is ISO-certified for quality in the purchase, storage, and sale of medical devices.
We support enduring alliances and ongoing relationship development. One of the key drivers of our success has been how we treat our clients and business partners.
They have extensive expertise introducing innovative medical devices to the CEE region, performing clinical trials that are either industry- or physician-initiated, obtaining CE certification, as well as feasibility and market research.
They do have experience with the entire cycle, from conception to the production of a finished product with clinical support that may subsequently be given to the patient.