Skip to content

Stopcocks 041209001A

by Argon Medical Devices, Inc.

Ref 041240002A, 041216000A

Active European Union. Also listed in GUDID (US), partly in commercial distribution.

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

None ongoing

1 closed

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/MDD EUDAMED NumberB-20886333201468 Basic UDI-DI Date10 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number20886333201468 UDI-DI Date9 Sep 2016ListedStatusListed GUDID: 2 of 3 UDI-DIs 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.

Recalls

1 recall · FDA

    • Terminated Z-0290-2020 FDA Class II initiated 16 Oct 2018 on shared 510(k) K780271

    The seal formed on the edge of the pouch may be incomplete, which could result in a loss of sterility to the product.

Recalls on a shared submission name another device cleared under the same FDA submission as this one.

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade Name
Stopcocks EUDAMEDGUDID
Stopcock GUDID
Generic Name
Intravenous line stopcock
Model / Ref / Catalog
041216000A, 041240002A, 041209001A
Primary DI / UDI-DI
20886333201468 EUDAMED
20886333201413 EUDAMED
00886333201372 GUDID
00886333201419 GUDID
00886333201464 GUDID
Basic UDI-DI
B-20886333201468, B-20886333201413
510(k) Number
FDA Product Code
DTL, KOC
EMDN Code
A0680 Drainage and fluid collection devices - accessories
GMDN Term
Intravenous line stopcock
Device Class
Class IIa EUDAMED
Class II GUDID
Regulation Number
870.4290, 876.5820
EU market of registration
Netherlands
GUDID distribution status
Not in Commercial Distribution (UDI-DI 00886333201372)
In Commercial Distribution (UDI-DI 00886333201419, 00886333201464)

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
20886333201468
20886333201413
GUDID
00886333201372
00886333201419
00886333201464
Device ClassEUDAMED
Class IIa
GUDID
Class II

Related devices

Cleared under the same submission (K780271)

Show all (10)

Other devices from Argon Medical Devices, Inc.

See all devices from Argon Medical Devices, Inc. →

Properties

  • Sterile
  • Single Use
  • Administering Medicine
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (15)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No