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Meridian

EUDAMED

Class IIa (EU MDR)

Ref 40013151Ref 40013150Ref 40013149

by EPflex Feinwerktechnik GmbH

Identity

Trade Name
Meridian EUDAMED
Device Name
Guidewires for Peripheral Application EUDAMED
Model / Reference
40013151 EUDAMED
40013150 EUDAMED
40013149 EUDAMED

Identifiers

Primary DI / UDI-DI
04255605607383 EUDAMED
04255605607369 EUDAMED
04255605607345 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

Meridian 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 (3)

  • EUDAMED 412c68f6-2c1e-4a55-acde-b4136fb6d212 61 fields · synced Aug 2, 2026
  • EUDAMED f8d69077-ef2f-4164-9cbe-970d1ac09917 61 fields · synced May 18, 2026
  • EUDAMED 4b6f4136-09ad-441e-9903-016f7337769c 61 fields · synced May 19, 2026