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Antal sidor, 252. Vikt, 0. Utgiven, 2013-02-28. ISBN, 9781573318549 Related Regulations · EU Medical Device Regulations · Selling a CE mark Class I Medical Device in Sweden - Any other requirements?

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i-medical builds workflow technologies to improve the efficiency and mobility of imaging diagnostics We strive to offer the benchmark solutions for process management and information sharing in the Imaging industry i-Medical ® products. i-Medical. products. All devices manufactured and marketed by i-Medical® meet the requirements of EU medical devices directive 93/42/EEC of 14 June 1993, the amendments directive 2007 47 EC of 29 March 2007, the German Medical Product Act (MPG), are registered with regulatory authorities in Germany, and bear the CE mark. i-Medical ® was founded in the year 2002 in Heidelberg, Germany, with the aim of manufacturing high-quality medical products and supplying them for ophthalmic surgery throughout the world. i-Medical ® is certified to ISO 9001 for the manufacture and distribution of ophthalmic products, and entitled to display the CE symbol under the number CE 0481 / CE 2460.

Download links: Copy / paste the snippet below to render the highlighted section on your page. Search medical terms and abbreviations with the most up-to-date and comprehensive medical dictionary from the reference experts at Merriam-Webster. Master today's medical vocabulary. Authoritative pronunciations. Medical I&I abbreviation meaning defined here.
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