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Peripheres Gefäß-Set Port Leiste

by Sengewald Klinikprodukte GmbH

Ref 66826683-04Model 66812137-15

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 Number4034393CPTCAR2AUT Basic UDI-DI 04034393692777UDI-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  • Withdrawn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
Fem-Pop Set
Model / Reference
66812137-15, 66826683-04
Primary DI / UDI-DI
04034393692777
Basic UDI-DI
4034393CPTCAR2AUT
EMDN Code
V010102 Scalpels without safety systems, single-use
Device Class
Class IIa
Medical Purpose
Sterile, disposable procedure pack, combination of devices for cardiac, thoracic, hybrid or vascular disease treatment.

Manufacturer details

EUDAMED SRN
DE-PR-000020748

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Properties

  • Sterile