ISO 14708-1 Implants for Surgery - Test Standard for Active Implantable Medical Devices

Material Testing

ISO 14708-1 Implants for Surgery - Test Standard for Active Implantable Medical Devices

ISO 14708-1 specifies generally applicable requirements for active implantable medical devices. The tests specified in ISO 14708 are type tests and will be performed on samples of an active implantable medical device to demonstrate conformity. ISO 14708-1 is applicable not only to electrically powered active implantable medical devices, but also to devices powered by other energy sources (e.g. gas pressure or springs). ISO 14708-1 is also applicable to certain non-implantable parts and accessories of active implantable medical devices.

ISO 14708-1 Implants for Surgery - Test Standard for Active Implantable Medical Devices

The device, commonly referred to as an active implantable medical device, may be a single device, a combination of devices, or a device or combination of devices and one or more accessories. It is not necessary for all of these parts to be partially or fully implantable, but some requirements for non-implantable parts and accessories need to be specified if they may affect the safety or performance of the implantable device.

EUROLAB assists manufacturers with ISO 14708-1 test compliance. Our test experts, with their professional working mission and principles, provide you, our manufacturers and suppliers, the best service and controlled testing process in our laboratories. Thanks to these services, businesses receive more effective, high-performance and quality testing services and provide safe, fast and uninterrupted service to their customers.

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