MAYFAIR DEVELOPMENTS S.A.S
Madame Natacha CHETRITT-BONNEYRAT

18 rue Sénac de Meilhan

17000 La Rochelle - France

+33 (0)5 46 28 74 41

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Certification & Communication 

Standard ISO 13485:2016

ISO 13485 is an international quality management standard that allows the implementation of regulatory requirements for medical devices and related services.

Standard ISO 13485:2016

ISO 13485 is an international quality management standard that allows the implementation of regulatory requirements for medical devices and related services.

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Standard ISO 13485:2016

ISO 13485 is an international quality management standard that allows the implementation of regulatory requirements for medical devices and related services.

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CE Médical Device Class IIa

The Medical CE according to the European Directive 93/42 / EEC Medical Devices is the official recognition that the certified device meets the safety and performance requirements imposed on health equipment, and guarantees that the benefit / risk has been clearly demonstrated.

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Abstract Clinic Study

Abstract of the retrospective clinical study published on March 21, 2019 by Dr. Gabrielle Cremer. Study demonstrating the performance and safety of the device in the treatment of tinnitus and hyperacusis.

Press Release

Mayfair Developments SAS Press Release
Presentation of the ØREBLUE® method to health professionals and the medical profession. March 22, 2019

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