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Insertion Set for use with Arrow(R) 4 Fr. PICC

by Arrow International LLC (Subsidiary of Teleflex Incorporated)

Ref EU-00740-45

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

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

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08019020000000000000236KP Basic UDI-DIDate22 Apr 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10801902199505 UDI-DIDate9 Nov 2022ListedStatusListed GUDID: in commercial distribution

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

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
Insertion Set for use with Arrow(R) 4 Fr. PICC EUDAMED
Arrow GUDID
Generic Name
Vascular catheterization support/maintenance kit, non-medicated
Device Name
Vascular Spring-Wire Guide Product
Model / Ref / Catalog
EU-00740-45, IPN920933
Primary DI / UDI-DI
10801902199505
Basic UDI-DI
08019020000000000000236KP
FDA Product Code
DQX
EMDN Code
A018003 Needle introducers
GMDN Term
Vascular catheterization support/maintenance kit, non-medicated
Device Class
Class III EUDAMED
Class II GUDID
Regulation Number
870.1330
Medical Purpose
The Arrow guidewires are intended to facilitate the placement of central circulatory system or peripheral vascular devices for diagnostic and interventional procedures.
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / ReferenceEUDAMED
EU-00740-45
GUDID
IPN920933
Device ClassEUDAMED
Class III
GUDID
Class II

Manufacturer details

EUDAMED SRN
US-PR-000023158

Other devices from Arrow International LLC (Subsidiary of Teleflex Incorporated)

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Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Convenience Kit
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No