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IMP Litholapixie-Führungsdraht

EUDAMED

Class IIa (EU MDR)

Ref 139802035070

by EPflex Feinwerktechnik GmbH

Identity

Trade Name
IMP Litholapixie-Führungsdraht EUDAMED
Device Name
Guidewires for Peripheral Application EUDAMED
Model / Reference
139802035070 EUDAMED

Identifiers

Primary DI / UDI-DI
04255605602807 EUDAMED
Basic UDI-DI
42556056gwcIIaFP EUDAMED
EMDN Code
U0602 UROLOGICAL GUIDEWIRES, NOT 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

IMP Litholapixie-Führungsdraht 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 b11b2fe9-1ab5-4236-9135-27b27259b047 61 fields · synced Jun 18, 2026