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Guidewires for Peripheral Application

EUDAMED

Class IIa (EU MDR)

Ref 40009605

by EPflex Feinwerktechnik GmbH

Identity

Device Name
Guidewires for Peripheral Application EUDAMED
Model / Reference
40009605 EUDAMED

Identifiers

Primary DI / UDI-DI
04255605603606 EUDAMED
Basic UDI-DI
42556056gwcIIaFP 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

CMR Substance

Yes

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Guidewires for Peripheral Application by Epflex Feinwerktechnik Gmbh — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
DE-MF-000005425

Sources (1)

  • EUDAMED 05ed4ab8-196c-48f9-bd0e-0d3191c37513 61 fields · synced Jun 18, 2026