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Pressure Monitoring Lines 040206005A

by Argon Medical Devices, Inc.

Ref 040206005A

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

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

None found

in data synced 22 Oct 2026

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-20886333201215 Basic UDI-DI 20886333201215UDI-DIDate28 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number20886333201215 UDI-DI Date9 Sep 2016ListedStatusListed 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.

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

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  • Withdrawn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
Monitoring Line EUDAMED
Pressure Monitoring Lines GUDID
Generic Name
Fluid transfer set, general-purpose
Model / Ref / Catalog
040206005A
Primary DI / UDI-DI
20886333201215 EUDAMED
00886333201211 GUDID
Basic UDI-DI
B-20886333201215
510(k) Number
FDA Product Code
DQO
EMDN Code
A0680 Drainage and fluid collection devices - accessories
GMDN Term
Fluid transfer set, general-purpose
Device Class
Class IIa EUDAMED
Class II GUDID
Regulation Number
870.1200
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
20886333201215
GUDID
00886333201211
Device ClassEUDAMED
Class IIa
GUDID
Class II

Related devices

Cleared under the same submission (K781558)

Show all (12)

Other devices from Argon Medical Devices, Inc.

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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