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Guidewire 395752

by Argon Medical Devices, Inc. EUDAMEDGUDID

Active European Union

Ref 395752Model 395271, 395654, 395573, 395610, 395746, 395752, 395798

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08863332700062N Basic UDI-DIDate2 Mar 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10886333211910 UDI-DIDate12 Sep 2016ListedStatusListed GUDID: not in commercial distribution

Coverage

2 jurisdictions

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  • Withdrawn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

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.

Recalls

0 recalls · FDA

No FDA recalls on record, checked 25 Oct 2026.

Specification

EUDAMED · GUDID

Trade Name
Guidewire
Generic Name
Peripheral vascular guidewire, manual
Model / Ref / Catalog
395752, 395271, 395654, 395573, 395610, 395746, 395798
Primary DI / UDI-DI
10886333211910 EUDAMED
00886333211913 GUDID
Basic UDI-DI
08863332700062N
Unit of Use DI
00886333211913
FDA Product Code
DQX
EMDN Code
A060299, C04020102
GMDN Term
Peripheral vascular guidewire, manual
Device Class
Class IIa EUDAMED
Class II GUDID
Regulation Number
870.1330
Market of Registration
Netherlands
GUDID distribution status
Not in Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
10886333211910
GUDID
00886333211913
Device ClassEUDAMED
Class IIa
GUDID
Class II

Other devices from Argon Medical Devices, Inc.

See all devices from Argon Medical Devices, Inc. →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (17)

  • 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
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No