\n Skip to content

Adjustable gastric band · Class IIb

MIDBAND™ — Adjustable Gastric Band Manufacturer

A proven and reversible solution

MIDBAND™ is a high-quality implantable medical device designed to provide an effective and customisable solution for the surgical treatment of severe obesity. The procedure is reversible.

The excess weight loss mentioned in the brief is approximately 50 to 61%, according to a prospective multicentre French study, DOI: 10.1007/s11695-011-0508-9.

Request technical information
MIDBAND™ — Adjustable Gastric Band Manufacturer

French manufacturing · ISO 13485 · CE MDR

Designed to support the procedure

01

Medical-grade silicone + titanium implantable port — latex- and phthalate-free

02

Low-pressure band, maximum fill volume 7 cc — 12 mm trocar

03

Fully radio-opaque for easier radiographic follow-up

04

Reversible procedure — no irreversible anatomical modification

05

Compatible with ambulatory surgery according to HAS criteria

06

Stabilised MIDPORT™ port, widened base, optional suture

Specifications and intended use

  • Radio-opaque bands
  • Flexible, soft and without an external rigid closure system
  • Sterile single-use device / do not reuse
  • Contains no latex or phthalates
  • Class IIb medical device
  • Made in France

Contraindications, adverse events, complications and residual risks: consult the notice at www.mid-ifu.com.

Open IFU / mid-ifu.com

Nutritional follow-up after gastric band placement

MID-CARE No. 2 was specifically formulated to support patients following restrictive surgery.

Discover MID-CARE

Answers for qualified professionals

Who manufactures the MIDBAND in France?

MIDBAND™ is designed and manufactured in France by MID, based in Dardilly near Lyon, since 1999. MID is ISO 13485 certified.

What is the difference between MIDBAND™ and Lap-Band?

According to the brief, MIDBAND™ combines low-pressure silicone, a maximum 7 cc volume, no external rigid closure system and the MIDPORT™ port.

How is the MIDBAND™ adjusted?

The band is adjusted by the surgeon through the subcutaneous MIDPORT™ implantable port. See the applicable IFU.