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pEGASUS Stent System

EUDAMED

Class III (EU MDR)

Ref PEGASUS-450-25Model Neurovascular Stent

by phenox GmbH

Identity

Trade Name
pEGASUS Stent System EUDAMED
Model / Reference
Neurovascular Stent EUDAMED
PEGASUS-450-25 EUDAMED

Identifiers

Primary DI / UDI-DI
04260123784706 EUDAMED
Basic UDI-DI
426012378NeuroStentTE EUDAMED
EMDN Code
P070402020102 NON-STAINLESS STEEL PERIPHERAL VASCULAR BARE METAL STENTS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Germany 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

pEGASUS Stent System by phenox 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
phenox GmbH
EUDAMED SRN
DE-MF-000006524

Sources (1)

  • EUDAMED 1af70012-7b1f-44d0-9447-ae2781394949 61 fields · synced Jun 20, 2026