Stryker develops, manufactures and markets a broad array of products and services that enable less-invasive care for some of the most threatening neurovascular conditions. Its prescription devices for use by healthcare professionals are regulated by government agencies in each of the countries in which it does business, such as the Food and Drug Administration in the United States (U.S.) or the Ministry of Health in Japan. These regulations often restrict the use of the information that can be disclosed to the public. If the format of the material presented is altered, the appropriate indications, contraindications, precautions, warnings and adverse events should be included.
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