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RoweInfuLine 2-fold

by RoweMed AG - Medical 4 Life EUDAMED

Active European Union

Ref A-2235, A-2229

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number42503476LEITUNGENGF Basic UDI-DIDate5 Apr 2022RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Leitungssysteme zur Injektion, Infusion und Ernährung
Model / Reference
A-2235, A-2229
Primary DI / UDI-DI
04250347604935, 04250347602771
Basic UDI-DI
42503476LEITUNGENGF
EMDN Code
C010180 Peripheral i.v. catheters and cannulas - accessories not included in other classes
Device Class
Class IIa
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005350

Other devices from RoweMed AG - Medical 4 Life

See all devices from RoweMed AG - Medical 4 Life →

Properties

Show properties
  • Sterile
Other properties (12)
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No