Australia has a mature and large - scale public and private healthcare system, and the demand for medical devices is also very strong. However, to sell, import, or export medical devices in Australia, it is necessary to complete the registration review and obtain an access certificate in accordance with relevant regulations. This article will introduce this process in detail.
On May 12, 2023, the Ministry of Food and Drug Safety (MFDS) of South Korea issued a notice to make some revisions to the Medical Device Manufacturing and Quality Control Standards to make it more in line with international standards. The main contents of the revisions include:
October 30, 2024, 14:15
Exporting medical devices to Malaysia requires meeting some specific certifications and requirements. The following are the certifications and precautions for exporting medical devices to Malaysia:
The Medical Device Product Export Sales Certificate is an approval document issued by the Drug Administration according to the application of enterprises within its jurisdiction for enterprises that meet the requirements. This certificate aims to facilitate the export of medical device products within its jurisdiction and is an important service item. The following will introduce the handling process and relevant precautions of the Medical Device Export Sales Certificate.
When exporting medical devices to the Russian market, understanding the relevant certification and market access requirements is crucial. Russian legislation and regulatory agencies for medical devices aim to ensure product safety and compliance. Below are the certification requirements to consider when exporting medical devices to Russia:
With the continuous development of medical technology, medical devices have become an indispensable part of modern healthcare. Many medical devices need to be imported from abroad, making it particularly important to understand the procedures and formalities for importing medical devices. In this article, we will introduce the definition, classification, and required import procedures for medical devices.
Importing dental medical equipment through agencies requires meeting specific conditions to ensure compliance with national regulations/quality standards and user safety/health protection.
Enterprises declaring the export of medical devices must ensure that the exported medical devices meet the requirements of the importing country (region). Generally, the exporting country does not inspect the goods.
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