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Uriblock D-Mannose effer

EUDAMED

Class IIa (EU MDR)

Ref 075112

by PK Benelux BV

Identity

Trade Name
Uriblock D-Mannose effer EUDAMED
Device Name
D-mannose Effervescent tablets EUDAMED
Model / Reference
075112 EUDAMED

Identifiers

Primary DI / UDI-DI
D-075112NK EUDAMED
Basic UDI-DI
B-075112NK EUDAMED
EMDN Code
G0499 ORALLY ADMINISTERED GASTROINTESTINAL DEVICES - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Croatia 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

Uriblock D-Mannose effer 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 b4c457c0-3f10-4e62-a277-0f390dc317df 61 fields · synced Aug 2, 2026