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HeltiQ Teekweg

EUDAMED

Class IIa (EU MDR)

Ref 145502

by Koninklijke Utermöhlen N.V.

Identity

Trade Name
HeltiQ Teekweg EUDAMED
Device Name
HeltiQ Tick Away EUDAMED
Model / Reference
145502 EUDAMED

Identifiers

Primary DI / UDI-DI
D-08717TD08-145502N35B EUDAMED
Basic UDI-DI
B-08717TD08-145502N35B EUDAMED
EMDN Code
Z120102 CRYOSURGERY EQUIPMENT 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

HeltiQ Teekweg by Koninklijke Utermöhlen N.V. — 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

EUDAMED SRN
NL-MF-000004873

Sources (1)

  • EUDAMED 1b5e5412-a82f-4da3-a43f-75f113689646 61 fields · synced Jun 17, 2026