Skip to content

Eopa™

by Medtronic, Inc. 4 variants

Ref 77522

Eopa (77522) is a medical device (EU MDD Class IIa; EMDN category extracorporeal circulation arterial cannulas) made by Medtronic, Inc., registered in EUDAMED on 9 Sep 2026 (Basic UDI-DI B-00199150023288), active as of 24 Oct 2026.

Active European Union

CE MDD

Valid until

No date given

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

Source EUDAMED, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-00199150023288 Basic UDI-DI Date9 Sep 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
EOPA™ Elongated One-Piece Art Cannula
Model / reference
77522
Primary DI / UDI-DI
00199150023288, 00763000135553
Basic UDI-DI
B-00199150023288, B-00763000135553
EMDN code
C0301040101 Extracorporeal circulation arterial cannulas, w/o filter
Device class
Class IIa
EU registration type
Legacy device (under a directive)
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
US-MF-000019977
Authorised representative
Medtronic B.V. NL-AR-000006050

Similar devices in this category

Other devices filed under EXTRACORPOREAL CIRCULATION CANNULAS.

Other devices from Medtronic, Inc.

See all devices from Medtronic, Inc. →

Properties

  • Supplied sterile
Other properties (13, all answered No)