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LimFlow V-Ceiver

EUDAMED

Class IIa (EU MDR)

Ref VC-CE-23Model VC-CE-21

by LimFlow SA

Identity

Trade Name
LimFlow V-Ceiver EUDAMED
Device Name
LimFlow V-Ceiver EUDAMED
Model / Reference
VC-CE-21 EUDAMED
VC-CE-23 EUDAMED

Identifiers

Primary DI / UDI-DI
00850017630451 EUDAMED
00850017630291 EUDAMED
Basic UDI-DI
0850017630VCCE21RS EUDAMED
EMDN Code
C010102 PERIPHERAL I.V. CATHETER SYSTEMS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

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

LimFlow V-Ceiver by LimFlow SA — Class IIa — 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 (2)

  • EUDAMED b7602cf8-81cc-480f-a0e6-55dfe61088cd 61 fields · synced Jul 12, 2026
  • EUDAMED aac8d6cf-e942-4017-9b53-645f309986ff 61 fields · synced May 19, 2026