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Artemis Neuro Evacuation Device 1.5 mm

EUDAMED

Class III (EU MDR)

Ref AP15Model Artemis Neuro Evacuation Device

by Penumbra, Inc.

Identity

Trade Name
Artemis Neuro Evacuation Device 1.5 mm EUDAMED
Device Name
Artemis Neuro Evacuation Device EUDAMED
Model / Reference
Artemis Neuro Evacuation Device EUDAMED
AP15 EUDAMED

Identifiers

Primary DI / UDI-DI
D-ArtemisBJ EUDAMED
Basic UDI-DI
B-ArtemisBJ EUDAMED
EMDN Code
A03010299 IRRIGATION CONTROLLERS - 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

Artemis Neuro Evacuation Device 1.5 mm by Penumbra, Inc. — 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
Penumbra, Inc.
EUDAMED SRN
US-MF-000008514
Authorised Representative
Penumbra Europe GmbH DE-AR-000004997

Sources (1)

  • EUDAMED 5aa3fb3f-5840-48a0-948a-f4cca916c152 61 fields · synced Jul 12, 2026