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Universal-Set III

by Sengewald Klinikprodukte GmbH

Ref 564523-1Model 66712058

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4034393CPTGEN1R9 Basic UDI-DI 04034393375311UDI-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  • Withdrawn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
Universal-Set
Model / Reference
66712058, 564523-1
Primary DI / UDI-DI
04034393375311
Basic UDI-DI
4034393CPTGEN1R9
EMDN Code
T0202 Surgical procedural kits (excluding surgical instrument kits)
Device Class
Class I
Medical Purpose
Sterile, disposable procedure pack, combination of devices for injury or disease treatment related to general surgery.

Manufacturer details

EUDAMED SRN
DE-PR-000020748

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Properties

  • Sterile