Skip to content

Revisions-Set

by Sengewald Klinikprodukte GmbH

Ref 66819152-11Model 66806578-25

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4034393CPTCAR3Q9 Basic UDI-DI 04034393695624UDI-DIDate8 May 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  • Withdrawn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

Device Name
ACVB-Set
Model / Reference
66806578-25, 66819152-11
Primary DI / UDI-DI
04034393695624
Basic UDI-DI
4034393CPTCAR3Q9
EMDN Code
T02010102 Incision drapes, with antibacterial agent
Device Class
Class III
Medical Purpose
Sterile, disposable procedure pack, combination of devices for cardiac, thoracic, hybrid or vascular disease treatment.

Manufacturer details

EUDAMED SRN
DE-PR-000020748

Other devices from Sengewald Klinikprodukte GmbH

See all devices from Sengewald Klinikprodukte GmbH →

Properties

  • Sterile