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Wirbelsäule dorsale ST und PLIF Set

by Sengewald Klinikprodukte GmbH

Ref 66826687-06

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 Number4034393CPTSPI3V9 Basic UDI-DI 04034393783581UDI-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  • Withdrawn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

Model / Reference
66826687-06
Primary DI / UDI-DI
04034393783581
Basic UDI-DI
4034393CPTSPI3V9
EMDN Code
H0199 Surgical sutures - other
Device Class
Class III
Medical Purpose
Sterile, disposable procedure pack, combination of devices for disease treatment related to spinal anesthesia or surgery.

Manufacturer details

EUDAMED SRN
DE-PR-000020748

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Properties

  • Sterile