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Diagnostic Solutions For Depression Medical Services In Usa California
6 services found
Manufactured by:Biomerica, Inc. based inIrvine, CALIFORNIA (USA)
Our policy is customer-focused and is certified by GMED SAS, the US FDA, and the European Union (CE mark). iomerica provides high quality medical diagnostic products that meet or exceed customer requirements and comply with all applicable regulatory requirements. Biomerica involves all employees in a continuous improvement process to increase productivity, improve quality and maintain the ...
Manufactured by:Ginolis Ltd based inOulunsalo, FINLAND
Ginolis provides design support to ensure that medical device and diagnostic designs are automation ready. The ability to identify and correct downstream issues will lead to reduced cycle time, higher product quality, and lower development and manufacturing costs. ...
by:Quy Technology Pvt Ltd based inGurgaon (Delhi NCR), INDIA
AI Recommendation engines today play an important role in helping businesses and customers have a better user experience. Product recommendations, movie suggestions, and people whom you would like to know on social media platforms are some of the popular examples of AI recommendation systems. With Quytech’s recommendation engine or system development services, we empower your business to ...
Manufactured by:Onda Corporation based inSunnyvale, CALIFORNIA (USA)
We provide general guidance, reporting, and measurements services for regulatory measurements in accordance with the IEC 60601 series ...
Manufactured by:Advanced Energy Industries, Inc. based inDenver, COLORADO (USA)
Shorten product development, increase reliability, and benefit from compliance expertise. Increased lifestyle conditions, patient lifespans, and outpatient procedures are transforming medical equipment. Equipment needs to be more mobile, include data storage and insight capabilities, and be more precise than ever. These requirements drive innovation and make shortened product development cycles ...
by:STEMart based inShirley, CALIFORNIA (USA)
CE marking is the manufacturer's declaration that their product complies technically and administratively with the essential regulatory requirements of Medical Device Directive 93/42/EEC (MDD) and its supplementary Directive 2007/47/EEC, Active Implantable Medical Devices Directive 90/385/EEC (AIMDD) and In Vitro Diagnostics Directive (IVDD) 98/79/EC, which outline the safety and performance ...