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Stemart Medical Device Services

5 services found

STEMart - Medical Device Design Services

STEMart - Medical Device Design Services

by:STEMart   based inShirley, CALIFORNIA (USA)
Medical device design is a complex sphere that includes creation and development of effective and life-improving tools and technologies aimed at reducing life risks and helping with medical equipment enhancement. Medical devices design is an important specific of product design, since numerous groundbreaking ...
CONTACT SUPPLIER

STEMart - Pilot Production Services of Medical Devices

STEMart - Pilot Production Services of Medical Devices

by:STEMart   based inShirley, CALIFORNIA (USA)
Processes close or equal to those to be used in production. Pilot production is a crucial process for devices that will be tested in clinical trials or pilot markets before transitioning to full-scale production. If the customer’s medical device is successful in a pilot market or clinical trial, it will likely transition to full- scale ...
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STEMart - Active Implantable Medical Device Testing Service

STEMart - Active Implantable Medical Device Testing Service

by:STEMart   based inShirley, CALIFORNIA (USA)
An active implantable medical device (AIMD) is any active medical device that is intended to be totally or partially introduced, surgically or medically, into the human body or by medical intervention into a natural orifice for diagnostic or therapeutic purposes, and which is intended to remain ...
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STEMart - Hip Joint Prostheses Testing Service

STEMart - Hip Joint Prostheses Testing Service

by:STEMart   based inShirley, CALIFORNIA (USA)
STEMart performs a variety of testing for partial and total hip joint prostheses to measure how they will withstand different levels of fatigue, compression, torsion, and bending over an extended period of time. ...
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STEMart - Notified Body (EU) Services

STEMart - Notified Body (EU) Services

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 ...
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