22/05/2025 Mobiles & Accessories
Switzerland Medical Device Registration is the official procedure by which medical devices must be approved for sale and distribution within the Swiss market. Following Switzerland's updated alignment with the EU Medical Device Regulation (EU MDR 2017/745) via its own Swiss Medical Device Ordinance (MedDO), all devices must meet strict safety, efficacy, and quality standards.As Switzerland is considered a “third country” to the EU post-Brexit and post-MRA updates, additional requirements, such as appointing a Swiss Authorized Representative (CH-REP) for foreign manufacturers, have been introduced.
Switzerland Medical Device Registration is the official procedure by which medical devices must be approved for sale and distribution within the Swiss...
Navigating the complex landscape of Medical Device Regulatory Services in Europe can be challenging for manufacturers and distributors alike. The Euro...
The global healthcare landscape is evolving rapidly, and this transformation is having a significant impact on the medical devices market. Technologic...
The Tunez CH01 Type C Fast Charger provides fast and efficient charging for all your compatible devices. Its lightweight and compact design makes it p...
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