KIJIMEA® REGULARIS

Primary DI

111388025018

Basic UDI-DI Code

PP07498KREG88

Reference

N/A

Device Types

Single use

Regulation

Eu Mdr

Classification

Eu Md Class 2b

Status

On The Market

Manufacturer

Synformulas GmbH

KIJIMEA® REGULARIS is an orally administered substance-based medical device for the treatment of poor digestion (constipation), bloated stomach, and bloating. KIJIMEA® REGULARIS contains methyl cellulose and simethicone as active ingredients. The device achieves its principal mode of action by acting locally in the gastrointestinal system. Methyl cellulose is a bulking agent and simethicone acts as a defoamer.

The Basic UDI-DI associated with this device has 3 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).