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Lucovital IBS

EUDAMED

Class IIa (EU MDR)

Ref 080307

by PK Benelux BV

Identity

Trade Name
Lucovital IBS EUDAMED
Device Name
Irritable Bowel Syndrome EUDAMED
Model / Reference
080307 EUDAMED

Identifiers

Primary DI / UDI-DI
D-080307NC EUDAMED
Basic UDI-DI
B-080307NC 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

Lucovital IBS 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 c5470c4c-2a06-4099-b677-f36061ddd973 61 fields · synced Jun 17, 2026