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Rayline

EUDAMED

Class III (EU MDR)

Ref AGW812137

by SWL Medizin GmbH

Identity

Trade Name
Rayline EUDAMED
Device Name
PTFE Coated Guidewire EUDAMED
Model / Reference
AGW812137 EUDAMED

Identifiers

Primary DI / UDI-DI
04251790221373 EUDAMED
Basic UDI-DI
B-04251790221373 EUDAMED
EMDN Code
C04020102 PERIPHERAL VASCULAR DIAGNOSTIC GUIDEWIRES, NON-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

Rayline 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 ba4107e1-857b-4f91-895f-59ca7165fc4a 61 fields · synced Jun 19, 2026