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Hydrophlic guidewire

EUDAMED

Class IIa (EU MDR)

Ref 46011994

by EPflex Feinwerktechnik GmbH

Identity

Device Name
Hydrophlic guidewire EUDAMED
Model / Reference
46011994 EUDAMED

Identifiers

Primary DI / UDI-DI
D-46011994A2 EUDAMED
Basic UDI-DI
B-46011994A2 EUDAMED
EMDN Code
U0601 UROLOGICAL GUIDEWIRES, HYDROPHILIC EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

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

Hydrophlic guidewire by Epflex Feinwerktechnik Gmbh — 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
DE-MF-000005425

Sources (1)

  • EUDAMED a27b2f1c-eba4-4d55-8a2a-37ca0aeff415 61 fields · synced Jun 18, 2026