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Superdrug IBS Relief

EUDAMED

Class IIa (EU MDR)

Ref 824709

by PK Benelux BV

Identity

Trade Name
Superdrug IBS Relief EUDAMED
Device Name
Irritable Bowel Syndrome EUDAMED
Model / Reference
824709 EUDAMED

Identifiers

Primary DI / UDI-DI
D-824709R6 EUDAMED
Basic UDI-DI
B-824709R6 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

Superdrug IBS Relief by PK Benelux BV — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
PK Benelux BV
EUDAMED SRN
NL-MF-000006672

Sources (1)

  • EUDAMED ea1904de-763e-4265-9142-74c1622eebbd 61 fields · synced Jul 22, 2026