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MS Set 2

by Sengewald Klinikprodukte GmbH

Ref 66731854Model 66728041-01

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 Number4034393CPTDER2AW2 Basic UDI-DI 04034393805917UDI-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  • Withdrawn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
Derma-Set
Model / Reference
66728041-01, 66731854
Primary DI / UDI-DI
04034393805917
Basic UDI-DI
4034393CPTDER2AW2
EMDN Code
A0380 Tubular devices - accessories
Device Class
Class IIa
Medical Purpose
Sterile, disposable procedure pack, combination of devices for disease alleviation related to dermatology.

Manufacturer details

EUDAMED SRN
DE-PR-000020748

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Properties

  • Sterile