ANSI/AAMI CI86:2017/(R)2025

ANSI/AAMI CI86:2017/(R)2025

Cochlear implant systems: Requirements for safety, functional verification, labeling and reliability reporting

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Details

This standard establishes minimum requirements for those active implantable medical devices known as cochlear implants or cochlear prostheses, which are intended to treat hearing impairment by means of electrical stimulation of the cochlea. Devices that treat hearing impairment other than by including electrical stimulation of the cochlea are not covered by this standard. This standard applies to the electrical stimulation component(s) of combination devices that treat hearing impairment using multiple means, including electrical stimulation. The tests specified in this standard are industry-accepted tests and are to be carried out on samples of devices to show compliance. This standard is also applicable to non-implantable parts and accessories of the devices, including fitting and diagnostic components. General and specific requirements are provided with regard to design verification, post-implantation device testing, reliability assessment and reporting, packaging and labeling, protections of the patient associated with design issues and device malfunctions, and protections of the device associated with environmental challenges arising from transport, storage, handling during implantation, unrelatedmedical treatments, and normal use. No annex

Zusätzliche Information

Autor Association for the Advancement of Medical Instrumentation (AAMI)
Veröffentlicht von AAMI
Document type Normen
Thema Implants & Artificial Organs
Datum der Bestätigung 2025-01-01
ICS 11.040.40 : Chirurgische Implantate, Prothesen und Orthesen
Seitenzahl 179
Ersetzt ANSI/AAMI CI86:2017
Schlagwort ANSI/AAMI CI86:2017/(R)2025
ANSI Approved