Identity
- Trade Name
- Activemed Reizdarmsyndrom EUDAMED
- Device Name
- Irritable Bowel Syndrome EUDAMED
- Model / Reference
- 073101 EUDAMED
Identifiers
- Primary DI / UDI-DI
- D-073101MY EUDAMED
- Basic UDI-DI
- B-073101MY EUDAMED
- EMDN Code
- G0401 ORALLY ADMINISTERED DEVICES FOR THE THERAPY OF GASTRO-INTESTINAL DISORDERS EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Netherlands EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
For individuals suffering from Irritable Bowel Syndrome (IBS), the Activemed Reizdarmsyndrom device offers a promising solution with its advanced medical technology and comprehensive user interface. Designed to meet the unique needs of patients, this device provides accurate diagnoses, precise measurements, and seamless administration of medications.
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-073101MY | Class IIa | Active |
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Manufacturer
- Manufacturer
- PK Benelux BV
- EUDAMED SRN
- NL-MF-000006672
Sources (1)
- EUDAMED 1a982a9a-34f3-4dee-8f76-61277bb007bb 61 fields · synced Jul 19, 2026