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LimFlow Stent Graft System

EUDAMED

Class IIb (EU MDR)

Ref RGS-40060-CE-24Model RGS-xxxx-CE-24

by LimFlow SA

Identity

Trade Name
LimFlow Stent Graft System EUDAMED
Device Name
LimFlow Stent Graft System EUDAMED
Model / Reference
RGS-xxxx-CE-24 EUDAMED
RGS-40060-CE-24 EUDAMED

Identifiers

Primary DI / UDI-DI
00850017630505 EUDAMED
Basic UDI-DI
0850017630RGSDDLLLCE24RT EUDAMED
EMDN Code
P0704020299 PERIPHERAL VASCULAR STENTS - OTHER EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Sutures

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

LimFlow Stent Graft System by LimFlow SA — Class IIb — 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
LimFlow SA
EUDAMED SRN
FR-MF-000011529

Sources (1)

  • EUDAMED 850b948b-0332-4d94-b4f8-6224149ec21f 61 fields · synced Jun 17, 2026