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Basic Information
- 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
Additional Description
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.
CND Nomenclature Codes
| Code | Description |
|---|---|
| G0401 | ORALLY ADMINISTERED DEVICES FOR THE THERAPY OF GASTRO-INTESTINAL DISORDERS |
Available In Countries
Related Devices
The Basic UDI-DI associated with this device has 3 devices in total. Below are some other devices sharing the same Basic UDI-DI.
Similar Devices
Other on-the-market devices with the same classification (Eu Md Class 2b) and regulation (EU MDR).