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Helix

EUDAMED

Class III (EU MDR)

Ref MDS809992Model MDS 3D

by SWL Medizin GmbH

Identity

Trade Name
Helix EUDAMED
Device Name
Detachable Coil System EUDAMED
Model / Reference
MDS 3D EUDAMED
MDS809992 EUDAMED

Identifiers

Primary DI / UDI-DI
04251790299921 EUDAMED
Basic UDI-DI
42517902MDS3DG2 EUDAMED
EMDN Code
Z12109001 DETACHABLE COIL EQUIPMENT FOR BRAIN ANEURYSMS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Türkiye EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

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

Helix by SWL Medizin GmbH — Class III — 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

Manufacturer
SWL Medizin GmbH
EUDAMED SRN
DE-MF-000008000

Sources (1)

  • EUDAMED af224073-c45a-4b2c-ad89-95c416b0048b 61 fields · synced Jul 8, 2026