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Lucovitaal Cranmed Once D

EUDAMED

Class IIa (EU MDR)

Ref 022253

by PK Benelux BV

Identity

Trade Name
Lucovitaal Cranmed Once D EUDAMED
Device Name
D-Mannose sachets EUDAMED
Model / Reference
022253 EUDAMED

Identifiers

Primary DI / UDI-DI
D-022253LS EUDAMED
Basic UDI-DI
B-022253LS EUDAMED
EMDN Code
G0499 ORALLY ADMINISTERED GASTROINTESTINAL DEVICES - OTHER 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

Lucovitaal Cranmed Once D 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 78fdbbc6-1bab-4854-815b-15ba39c5a72a 61 fields · synced Jul 9, 2026