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APO D-mannose lacto 10 s

EUDAMED

Class IIa (EU MDR)

Ref 13899

by PK Benelux BV

Identity

Trade Name
APO D-mannose lacto 10 s EUDAMED
Device Name
D-Mannose & Lactobacillus EUDAMED
Model / Reference
13899 EUDAMED

Identifiers

Primary DI / UDI-DI
D-13899H3 EUDAMED
Basic UDI-DI
B-13899H3 EUDAMED
EMDN Code
G0499 ORALLY ADMINISTERED GASTROINTESTINAL DEVICES - OTHER EUDAMED

Classification

Device Class
Class IIa 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

APO D-mannose lacto 10 s 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 e231996c-3f93-42e0-967c-f1c10bbc2678 61 fields · synced Jul 9, 2026