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Amecath Arterial Catheter Kit

by Ameco medical industries 22 variants

Ref AL-0508-KSDModel As attached in the Declaration of conformity

Active European Union

CE MDR

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/MDR Number6221139INV-ART-2aGM Basic UDI-DI 06221139270186UDI-DIDate23 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  • Withdrawn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/MDR Active

Specification

EUDAMED

Model / Reference
As attached in the Declaration of conformity, AL-0508-KSD
Primary DI / UDI-DI
06221139270186
Basic UDI-DI
6221139INV-ART-2aGM
Direct Marketing DI
06221139270186
EMDN Code
C0504 Arterial introduction sets
Device Class
Class IIa
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
EG-MF-000028383
Authorised representative
Obelis s.a. BE-AR-000000106

Other devices from Ameco Medical Industries

See all devices from Ameco Medical Industries →

Properties

  • Sterile

Other properties (12)

  • 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