2025年2月17日 · As required by regulations, CE marking certificates are mandatory to put medical devices on the European market. GMED, as a notified body, identification number CE 0459, supports you through the certification process, sharing with you its expertise and know-how in the medical device industry.

Learn more about GMED and their medical device certification worldwide, meeting the requirements of European Medical Device Regulations.

Learn more about GMED's About Us and how they serve the medical device industry worldwide to meet the new requirements of European medical device regulations.

GMED（CE 0459）刚刚被 法国国家药品和健康产品安全局 （ANSM）指定为欧盟又一家具有体外诊断（IVDR）审核资质的公告机构。 因此，GMED从2021年8月20日起被授权根据（欧盟）2017/746号条例向制造商提供认证服务。 随着（欧盟）2017/746号条例于 2022年5月26日 生效，为了应对合格评估请求的强劲增长，GMED在其官网上表示，他们将继续部署其发展战略，投资于专家资源，加速其工具和流程的数字化，同时巩固其支持每个认证项目的方法，以便为其客 …

GMED is a leading Certification Organization and a distinguished Notified Body (CE0459) and assesses the conformity of medical devices and in vitro diagnostic medical devices in accordance with...

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Globus Medical, Inc. operates as a medical device company that develops and commercializes healthcare solutions. The firm engages in developing products that promote healing in patients …