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PTFE Guidewire J3-tip

EUDAMED

Class III (EU MDR)

Ref 49012948

by EPflex Feinwerktechnik GmbH

Identity

Device Name
PTFE Guidewire J3-tip EUDAMED
Model / Reference
49012948 EUDAMED

Identifiers

Primary DI / UDI-DI
D-49012948BM EUDAMED
Basic UDI-DI
B-49012948BM EUDAMED
EMDN Code
C0499 CARDIOVASCULAR GUIDEWIRES - OTHER EUDAMED

Classification

Device Class
Class III 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

PTFE Guidewire J3-tip by Epflex Feinwerktechnik Gmbh — Class III — 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 5d9d024e-f99c-4957-8be5-d2a4c23afa33 61 fields · synced Jun 19, 2026