Celeris 3d Vision vs connectgo.pro by ottobock.

This app uses the Structure SDK / TrueDepth camera for 3D scanning. Supported device list (updated regularly): https://techmed3d.zohodesk.com/portal/en/kb/articles/minimun-device-requirements La aplicación Celeris 3D Vision, es una solución portátil, versátil y fácil de usar para la toma de medidas y digitalización 3D del cuerpo humano. Podrás enviar de manera inmediata a nuestra Central de Fabricación CFAB, permitiéndote una fabricación de tus productos de manera más eficiente en tiempos y reduciendo tus costes. Realiza un escaneo fácil y rápido gracias a nuestro escáner Celeris 3D. Con una interfaz intuitiva y ergonómica que permite un proceso de escaneo simple y eficaz. Celeris 3D Vision combinado con nuestro escáner Celeris 3D está especialmente adaptado para escanear: pie, pierna, rodilla, torso, tronco, cabeza, superficie plantar y espumas fenólicas para plantillas. La CFAB de Celeris trabaja para ti, reduce costes y dedica tu tiempo y tu equipo a generar negocio.

connectgo.pro by ottobock. allows O&P professionals to install microprocessor-controlled prostheses and orthoses for lower limbs according to the needs and mobility of the patient. Therapists can adjust the settings of certain prostheses in some areas and use feedback functions for training purposes. The additional functions are: - Standard behaviour setting for prostheses and orthoses - MyModes settings for special movement patterns and situations - Calibration or static measurement and optimisation - Status information display The instructions for use are available online https://product-documents.ottobock.com/IFU/INT/560X29-2/647G1834/01/O/S/F Manufacturer: Otto Bock Healthcare Products GmbH Brehmstraße 16 · 1110 Vienna · Austria T +43 1 523 37 86 · F +43 1 523 22 64 www.ottobock.com This product complies with the applicable European regulations for medical devices. Jurisdiction statement: The app is only available for use in countries where the corresponding medical device hardware has regulatory clearance to be used, such as: EU countries, EFTA countries, UK, USA, Canada, Australia, New Zealand. The app and medical device hardware is not cleared for use in jurisdictions where regulatory approval has not been obtained. We are required to remind you to seek advice from a medical professional as well as using this app and before coming to any medical conclusions.