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Pressure Injectable Two-Lumen PICC

by Arrow International LLC (Subsidiary of Teleflex Incorporated) 23 variants

Ref EU-24052-IR

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number08019020000000000000043KA Basic UDI-DI 10801902187021UDI-DIDate16 Jun 2026RegisteredStatusActive

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  • Withdrawn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
PICC Procedure Pack
Model / Reference
EU-24052-IR
Primary DI / UDI-DI
10801902187021
Basic UDI-DI
08019020000000000000043KA
EMDN Code
C01020102 Central i.v. multi-lumen catheters, peripheral access
Device Class
Class III
Medical Purpose
A Peripherally inserted Central Catheter permits venous access to the central circulation through a peripheral vein. It offers an alternative method of intravenous therapy and allows for central venous pressure monitoring for select adult and pediatric patients.

Manufacturer details

EUDAMED SRN
US-PR-000023158

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Properties

  • Sterile