KIJIMEA® IBS PRO

Primary DI

111972441010

Basic UDI-DI Code

PP07498KPRO16

Reference

n.a.

Device Types

Single use

Regulation

Eu Mdr

Classification

Eu Md Class 2b

Status

On The Market

Manufacturer

Synformulas GmbH

Kijimea® IBS PRO is a medical device that contains the heat-inactivated Bifidobacteria strain B. bifidum HI-MIMBb75. It is intended to be used for the treatment of irritable bowel syndrome with the typical symptoms of constipation, diarrhoea, abdominal pain, flatulence, and bloating.

The Basic UDI-DI associated with this device has 19 devices in total. Below are some other devices sharing the same Basic UDI-DI.

Other on-the-market devices with the same classification (Eu Md Class 2b) and regulation (EU MDR).