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Peripheral Guidewire

EUDAMED

Class III (EU MDR)

Ref PAGW827539

by SWL Medizin GmbH

Identity

Device Name
Peripheral Guidewire EUDAMED
Model / Reference
PAGW827539 EUDAMED

Identifiers

Primary DI / UDI-DI
04251790275390 EUDAMED
Basic UDI-DI
B-04251790275390 EUDAMED
EMDN Code
C04020101 PERIPHERAL VASCULAR DIAGNOSTIC GUIDEWIRES, HYDROPHILIC EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Türkiye 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

Peripheral Guidewire by SWL Medizin 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

Manufacturer
SWL Medizin GmbH
EUDAMED SRN
DE-MF-000008000

Sources (1)

  • EUDAMED 593d426b-edd3-4718-b9a8-d88508b17049 61 fields · synced Jun 18, 2026