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Arrowg+ard Blue(R) Two-Lumen CVC

by Arrow International LLC (Subsidiary of Teleflex Incorporated) United States EUDAMED

Ref CV-26702-E EMDN C01020202

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number08019020000000000000044KC Basic UDI-DIDate8 Jun 2026RegisteredStatusActive

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  • Withdrawn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 · synced 25 Oct 2026

Device Name
AGB CVC Procedure Pack
Model / Reference
CV-26702-E
Primary DI / UDI-DI
10801902178890
Basic UDI-DI
08019020000000000000044KC
EMDN Code
C01020202 Central venous double-lumen catheters, non-tunneled
Device Class
Class III
Medical Purpose
The Arrow catheter is indicated to permit short-term (< 30 day) central venous access for the treatment of diseases or conditions requiring central venous access, including, but not limited to the following: • Lack of usable peripheral IV sites • Central venous pressure monitoring • Total parenteral nutrition (TPN) • Infusions of fluids, medications, or chemotherapy • Frequent blood sampling or receiving blood transfusions/blood products • Injection of contrast media When used for pressure injection of contrast media, do not exceed the maximum indicated flow rate for each catheter lumen. The maximum pressure of power injector equipment used with the pressure injectable CVC may not exceed 400 psi.

Manufacturer details

EUDAMED SRN
US-PR-000023158

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Properties & raw data

Show properties, registry sources and raw records
  • Sterile

Sources (1)

  • EUDAMED 10801902178890|08019020000000000000044KC 61 fields · synced 25 Oct 2026