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Active Implantable Medical Devices Services
8 services found
by:TÜV Rheinland AG based inKöln, GERMANY
High-quality, active implantable medical devices, such as pacemakers or cochlear implants, give patients new quality of life. EU Directive 90/385/EEC defines the requirements for active implantable medical devices on the European market. As a ...
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 ...
Manufactured by:Atrotech Oy based inTampere, FINLAND
Design, development and design transfer of Active Implantable Medical Devices (AIMD) Implanted electronics - Lead wires -Electrodes, Manufacturing of AIMDs, Wireless power transmission to implanted electronics Short-range bidirectional telemetry, System design and integration Biomedical - ...
by:European Device Solutions Limited based inWhitley Bay, UNITED KINGDOM
The new Medical Device Regulation (MDR) comes into force on the 26th May 2021 replacing the Medical Devices Directive (MDD) and the Active Implantable Medical Devices Directive (AIMDD). The MDR applies to all manufacturers selling medical ...
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 ...
Manufactured by:UroMems based inGrenoble, FRANCE
UroMems’s ambition is to revolutionize the treatment for severe urinary incontinence using the latest technological advances in the field of embedded systems and micro-technologies for the development of its implantable ...
by:SustChem Engineering S.A. based inAthens, GREECE
CE Marking is the symbol as shown on the top of this page. The letters 'CE' are the abbreviation of the French phrase 'Conformité Européene' which literally means 'European Conformity'. The term initially used was 'EC Mark' and it was officially replaced by 'CE Marking' in the Directive 93/68/EEC in 1993. 'CE Marking' is now used in all EU official ...
by:Metecon GmbH based inMannheim, GERMANY
An audit is the most effective method to establish certainty that you as the manufacturer or distributor of medical devices are in the position to meet all requirements. Metecon offers comprehensive support in this regard with a wealth of experience and know-how. Take a moment to get an overview of our services. And if you see any need, we look forward to discussing a solution with ...