← Back to catalogue

p48 LITE Flow Modulation Device

EUDAMED

Class III (EU MDR)

Ref P48-LT-250-9Model Neurovascular Flow Diverter

by phenox GmbH

Identity

Trade Name
p48 LITE Flow Modulation Device EUDAMED
Model / Reference
Neurovascular Flow Diverter EUDAMED
P48-LT-250-9 EUDAMED

Identifiers

Primary DI / UDI-DI
04260123785765 EUDAMED
Basic UDI-DI
426012378FlowDiverterSV 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

Yes

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

p48 LITE Flow Modulation Device 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
phenox GmbH
EUDAMED SRN
DE-MF-000006524

Sources (1)

  • EUDAMED 063028f7-7591-4b97-b38c-ece442ce1882 61 fields · synced Jun 20, 2026