Bariatric surgery is performed within a multidisciplinary care pathway. MID develops and manufactures devices used by qualified healthcare professionals for several established procedures.
Adjustable gastric banding
MIDBAND™ is an implantable, adjustable and reversible gastric band. Its design combines medical-grade silicone with the titanium implantable port. The maximum fill volume is 7 cc and the required trocar is 12 mm.
Sleeve gastrectomy
MIDSLEEVE™ is an orogastric calibration tube with an orientable balloon up to 75 ml. It is designed to support precise and reproducible calibration during sleeve gastrectomy and can be connected to suction for leak testing after stapling.
Gastric bypass
MIDCAL™ is a medical-grade silicone calibration ring offering four adjustments: 65, 70, 75 and 80 mm. It helps calibrate the gastric pouch and remains in place after placement. MID-TUBE™ and MIDSOND support calibration needs in bariatric procedures.
Quality and clinical collaboration
MID has been designing and manufacturing in France since 1999. Its quality system is certified to ISO 13485, with CE and international regulatory pathways. Present from listening to clinical needs through to commercialisation, the R&D department applies Verification and Validation procedures.
Choosing the right device
The choice of device depends on the procedure, the surgeon’s technique, the patient pathway and the instructions for use. Product specifications and contraindications must always be reviewed in the applicable instructions for use at www.mid-ifu.com.
Questions & answers
A clear framework for healthcare professionals
Which devices support sleeve gastrectomy?
MIDSLEEVE™ is a calibration probe dedicated to sleeve gastrectomy. The applicable instructions for use must be reviewed by qualified healthcare professionals.
Which ring is used for gastric bypass calibration?
MIDCAL™ is the calibration ring described for banded gastric bypass. It offers four adjustments.
Is MID certified by HAS?
The MID quality system is ISO 13485 certified. HAS is a French health authority and is not a certification body for MID; regulatory information must be checked in the applicable documents.
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.
MIDSOND is a Class I.s medical device manufactured by MEDICAL INNOVATION DEVELOPPEMENT (MID) SAS – CE n°0459. MIDSOND is a sterile medical device. 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.