Quality, proximity and measured decisions support a more sustainable medical device pathway.
Concrete commitments
Actions that turn principles into practice
Risk prevention and improved working conditions
Work-life balance and individual training plans
Diversity, inclusion and open social dialogue
Clear code of conduct and anti-corruption policy
Fair commercial practices and responsible suppliers
Sustainable transport, short supply chain and waste reduction
REGULATORY INFORMATION
MIDBAND™ is a Class II.b medical device manufactured by MEDICAL INNOVATION DEVELOPPEMENT (MID) SAS – CE n°0476. MIDBAND™ is a sterile medical device, intended for implantation in the human body. It must only be handled by practitioners with experience of bariatric surgery.
Information réglementaireDispositifs médicaux · ISO 13485 · CE
Ce site présente des dispositifs médicaux et chirurgicaux soumis au Règlement (UE) 2017/745. Leur consultation est réservée aux professionnels de santé.