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Tilman

EUDAMED

Class I (EU MDR)

Ref 614789Ref 073743

by PK Benelux BV

Identity

Trade Name
Tilman EUDAMED
Device Name
Tilman Eucalyptus forte EUDAMED
Model / Reference
614789 EUDAMED
073743 EUDAMED

Identifiers

Primary DI / UDI-DI
D-614789QR EUDAMED
D-073743PE EUDAMED
Basic UDI-DI
B-614789QR EUDAMED
B-073743PE EUDAMED
EMDN Code
Q030103 NASAL IRRIGATION SOLUTIONS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Bulgaria EUDAMED
Belgium 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

Tilman by PK Benelux BV — Class I — 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 (2)

  • EUDAMED 32b558cd-9584-4cc8-8185-ff3f3e9d1f6f 61 fields · synced Jul 15, 2026
  • EUDAMED 4ddc532c-07d9-4dc7-884c-01bffbb3f82f 61 fields · synced May 18, 2026