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Haut-Desinfektions-Set

by Paul Hartmann AG 12 variants

Ref 4791732Model 3307

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number40495003307KJ Basic UDI-DI 04052366978499UDI-DIDate27 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  • Withdrawn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
Care set Pre-op preparation
Model / Reference
3307, 4791732
Primary DI / UDI-DI
04052366978499
Basic UDI-DI
40495003307KJ
EMDN Code
V9099 Various devices not included in other classes - other
Device Class
Class III
Medical Purpose
A MediSet is the compilation of defined components used to perform a medical care. The components are single-used products and are used together to perform a medical care.

Manufacturer details

EUDAMED SRN
DE-PR-000019925

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Properties

  • Sterile