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COR-VALV Atrial retractor

by Coroneo Inc. 2 variants

Ref 1010723

COR-VALV Atrial retractor (1010723) is a Class IIa device made by Coroneo Inc, registered in EUDAMED on 31 Jul 2026 (Basic UDI-DI B-1010723TX), withdrawn as of 24 Oct 2026.

Withdrawn Withdrawn in European Union. No longer placed on the EU market.

Was authorized under CE MDD, withdrawn

Ended

Withdrawn

Date not published (CE MDD)

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-1010723TX Basic UDI-DI D-1010723TXUDI-DIDate31 Jul 2026RegisteredStatusWithdrawn No longer placed on the EU market

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Withdrawn

Specification

EUDAMED

Model / reference
1010723
Primary DI / UDI-DI
D-1010723TX
Basic UDI-DI
B-1010723TX
EMDN code
L07070202 Cardiac retractors, reusable
Device class
Class IIa
EU registration type
Legacy device (under a directive)

Manufacturer details

EUDAMED SRN
CA-MF-000019141
Authorised representative
Obelis s.a. BE-AR-000000106

Similar devices in this category

Other devices filed under CARDIAC DILATORS AND RETRACTORS, REUSABLE.

Other devices from Coroneo Inc

See all devices from Coroneo Inc →

Properties

  • Sterilise before use
  • Reusable
Other properties (10, all answered No)