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SuperDrug Wind relief

EUDAMED

Class IIa (EU MDR)

Ref 824133

by PK Benelux BV

Identity

Trade Name
SuperDrug Wind relief EUDAMED
Device Name
Gas & Bloating EUDAMED
Model / Reference
824133 EUDAMED

Identifiers

Primary DI / UDI-DI
D-824133Q5 EUDAMED
Basic UDI-DI
B-824133Q5 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 Wind 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 d10fdfa4-f89e-416b-913d-f6f87b868fa8 61 fields · synced Jun 20, 2026