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Guidwire J3-FC-090/10M-035

EUDAMED

Class IIa (EU MDR)

Ref 46012027

by EPflex Feinwerktechnik GmbH

Identity

Device Name
Guidwire J3-FC-090/10M-035 EUDAMED
Model / Reference
46012027 EUDAMED

Identifiers

Primary DI / UDI-DI
D-460120278D EUDAMED
Basic UDI-DI
B-460120278D 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

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

Guidwire J3-FC-090/10M-035 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 b022394b-6d5d-4c79-8847-148fa54a3849 61 fields · synced Aug 3, 2026