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In which countries is the CE marking required?

 · The CE marking will be accepted during a transition period that ends on 1-1-2023. b) Switzerland is not a member of the European Union, but for some products it accepts the CE marking as a presumption of conformity with Swiss national technical regulations. c) Turkey is neither member of the EU, nor is considered a part of the EEA.

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Micro Medical Devices is a technology company that specializes in developing portable, handheld technology to help solve day-to-day challenges for a new generation of eye care practitioners. We're led by a team of engineers, designers, and clinical experts, committed to combining our expertise for the benefit of the people who use our products.

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Product Code Classification Database | FDA

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SAE International is the global leader in technical learning for the mobility industry. Whether you are an engineer or business professional looking to advance your career, or an educator in search of creative and effective ways to engage students in …

SAE International

SAE International is the global leader in technical learning for the mobility industry. Whether you are an engineer or business professional looking to advance your career, or an educator in search of creative and effective ways to engage students in …

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ROCHESTER, N.Y., Dec. 14. Carestream Health Improves Service Delivery for Customers in Medical Imaging. Carestream Health recently completed a significant company-wide business transformation aimed at improving service delivery and support to its medical/radiology customers, which in turn helps them to provide more reliable and complete imaging support for …

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CE marking

CE marking is a part of the EU's harmonisation legislation, which is mainly managed by Directorate-General for Internal market, Industry, Entrepreneurship and SMEs. The CE marking for Restriction of Hazardous Substances is managed by Directorate-General for Environment Search for available translations of the preceding link EN •••.

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BSI Medical Devices offers certification services to support your global market access goals. We are: A designated EU Notified Body. A UK Approved Body. An accredited ISO 13485 Certification Body. A recognized Auditing Organization under the Medical Device Single Audit Program (MDSAP) A recognized Certification Body in many global markets.