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Argyle™ Dialysis Catheter Accessory J/Straight Stainless Steel Guidewire 0.035" x 27.7" (0.89 mm x 70 cm)

by Mozarc Medical US LLC

Ref 8817231001Model Argyle™ Dialysis Catheter Accessory J/Straight Stainless Steel Guidewire

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-20884521004020 Basic UDI-DI 20884521004020UDI-DIDate3 Sep 2026RegisteredStatusActive

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

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Model / Reference
Argyle™ Dialysis Catheter Accessory J/Straight Stainless Steel Guidewire, 8817231001
Primary DI / UDI-DI
20884521004020
Basic UDI-DI
B-20884521004020
EMDN Code
F900101 Peritoneal dialysis catheters and kits
Device Class
Class IIa
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
US-MF-000043425
Authorised representative
Mozarc Medical Ireland Ltd. IE-AR-000048547

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Properties

  • Sterile

Other properties (10)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No