Ottobock Professionals.
Information for Professionals.
Learn about products, education, and business resources that help maximise patient outcomes and clinical success. Our website for professionals has what you need.
Ottobock Academy
Meet the UK Academy team, our field based staff who are dedicated to managing the Ottobock product training needs of our UK customers.
Meet the UK Academy team, our field based staff who are dedicated to managing the Ottobock product training needs of our UK customers.
Back to Mobility
After a lower limb amputation, restoring a patient’s mobility is a complex process that should always be guided by a clinical specialist like you. The following pages were designed to help you deepen your technical expertise, personalise post-amputation therapy, and pursue the best possible outcomes for each of your patients.
After a lower limb amputation, restoring a patient’s mobility is a complex process that should always be guided by a clinical specialist like you. The following pages were designed to help you deepen your technical expertise, personalise post-amputation therapy, and pursue the best possible outcomes for each of your patients.
After Sales Support
Our Customer Support Team is here to assist you and meet the needs of your patients. Access comprehensive information on product trials, loaners, service and repairs, along with guidance for returns and placing orders.
Our Customer Support Team is here to assist you and meet the needs of your patients. Access comprehensive information on product trials, loaners, service and repairs, along with guidance for returns and placing orders.
MDR Suite
The following webpage focuses on the new Medical Device Regulation 2017/745 (MDR) for manufacturers of custom-made devices. This new Medical Device Regulation 2017/745 (MDR) will play a significant role in patient care providers that create products like prosthetics, orthotics or wheelchairs.
The following webpage focuses on the new Medical Device Regulation 2017/745 (MDR) for manufacturers of custom-made devices. This new Medical Device Regulation 2017/745 (MDR) will play a significant role in patient care providers that create products like prosthetics, orthotics or wheelchairs.
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