Our history
Medical innovation since 1999
MID (Medical Innovation Development) provides healthcare professionals with medical devices that meet demanding quality requirements. Innovation is part of the company culture, with active research and development projects focused on better answering clinical needs.
25+
+25
60+
ISO
Featured device
MIDBAND™
adjustable gastric band, made in France and designed for qualified bariatric surgeons.
Our journey since 1999
Milestones in MID’s development
MID SAS founded
MIDBAND (ref. MID001)
MIDSLEEVE (ref. MID160)
MIDBAND (ref. MID100-M)
TFDA approval (Taiwan)
MIDCAL (ref. MID180)
MID-TUBE (ref. MID130)
MID-TUBE (ref. MID136)
MID-TUBE (ref. MID131)
CFDA approval (Korea)
MID-VET (ref. MID300V)
Metropolitan France distribution — SEJONG Medical monotrocart
French distribution of the REACH SURGICAL stapling range
Distribution of the BLUESAIL+ SURGICAL range
Our vocation
MID provides healthcare professionals with medical devices that meet demanding quality requirements.
Innovation is part of our culture. Active research and development projects help us answer clinical needs more precisely.
Our collaborations
We collaborate with clinical and scientific experts. Our R&D department applies Verification and Validation procedures from the idea to industrialisation and commercialisation.
We hold more than 60 patents and trademarks.
Our international presence
In France, MID is one of the recognised players in medical devices dedicated to bariatric surgery. The company is present in more than 25 countries and a significant share of its activity is international.
DARDILLY · FRANCE
Made close to our teams
Design, development, quality, regulatory affairs and logistics are coordinated from the MID site near Lyon.
Our values
The principles that guide MID
01
Adaptability
Innovation is part of our culture, with an active R&D pipeline focused on professional healthcare needs.
02
Proximity
Co-development with clinical experts, from the idea to industrialisation.
03
Expertise
Design in Dardilly using 3D modelling, numerical simulation and 3D printing.
04
Reliability
ISO 13485, CE, Taiwan, Australia and UK quality requirements with controlled traceability.
Quality commitments
Quality is designed into every stage
Our quality policy is based on listening to customers, regulatory compliance and continuous improvement.
01
Customer listening
Understand needs, validate proposed solutions and improve product performance and safety.
02
Compliance
Meet regulatory and normative requirements and mobilise the company around good practices.
03
ISO 13485
A quality management system for medical devices.
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.
MIDCAL™ is a Class II.b medical device manufactured by MEDICAL INNOVATION DEVELOPPEMENT (MID) SAS – CE n°0476. MIDCAL™ is a sterile medical device, intended for implantation in the human body. It must only be handled by practitioners with experience of bariatric surgery.
MID-TUBE™ is a Class II.a medical device manufactured by MEDICAL INNOVATION DEVELOPPEMENT (MID) SAS – CE n°0459. MID-TUBETM is a sterile medical device. It must only be handled by practitioners with experience of bariatric surgery.
MIDSLEEVE™ is a Class II.a medical device manufactured by MEDICAL INNOVATION DEVELOPPEMENT (MID) SAS – CE n°0459. MIDSLEEVETM is a sterile medical device. It must only be handled by practitioners with experience of bariatric surgery.
