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Insertion Kit-Arterial

by Eurosets S.R.L.

Ref EURIK80A

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805210922EURIK180V48 Basic UDI-DI 08052109222229UDI-DIDate17 Oct 2023RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Insertion Kit
Model / Reference
EURIK80A
Primary DI / UDI-DI
08052109222229
Basic UDI-DI
805210922EURIK180V48
EMDN Code
C0180, C0499
Device Class
Class III
Medical Purpose
The Insertion Kit is intended as a complete kit of access to vascular system and has the function to provide safe and comfortable catheter and cannulae insertions. The Insertion Kit is composed by: • INSERTION SET manufactured and EC marked by Eurosets (scalpel blade, introducer needle, syringe and dilators set), • Guidewire manufactured and EC marked by Merit.

Manufacturer details

EUDAMED SRN
IT-PR-000027598

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See all devices from Eurosets S.R.L. →

Properties

Other properties (1)

  • Sterile: No