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Implant Device Services In Europe
10 services found
by:Endo Endoengineering Srl based inFalconara Marittima, ITALY
The DM 21 December 2009 establishes the obligation to register in the medical devices database uses new methods. Registration is mandatory for all manufacturers and other entities responsible for placing devices on the Italian market for Class I, IIa, IIb and III, kits and assemblies and active implantable ...
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 devices into Europe and requires them to update both their processes and ...
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 notified body, we conduct conformity assessments for your active ...
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 ...
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 - Mechanical - Electrical, Established ...
Manufactured by:Lattice Medical based inLoos, FRANCE
Lattice Medical is developing the first ISO 13485 production in clean room with 3D printing for designing personalized implantable resorbable medical devices. This unique platform is endowed with new 3D printing and extrusion technology that is able to produce prototypes, pre-series and industrial series for R&D trials, pre-clinical and clinical studies at ...
Manufactured by:Winncare Group based inPresteigne, UNITED KINGDOM
Environment and ISO 14001 certification; The AskleSanté manufacturing site has been located in an industrial area in Grézan in Nîmes since 1995. Specialising in the design and manufacture of medical devices for the prevention and treatment of bedsores, the manufacturing and storage units are classified under the Approval regime in accordance with Classified Installation ...
Manufactured by:S3 Connected Health based inDublin, IRELAND
Creating digital health solutions around wearable and implantable medical devices allows for the collection of data that will unlock the full value of these devices and improve patient and clinician ...
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 ...