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Pack universel

by Paul Hartmann AG

Ref 2335051Model 3142

Active European Union

CE MDR

Valid until

No date given

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number40495003142KA Basic UDI-DI 04099467017962UDI-DIDate27 May 2026RegisteredStatusActive EUDAMED: not on the EU market

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  • Withdrawn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
CombiSet General surgery
Model / reference
3142, 2335051
Primary DI / UDI-DI
04099467017962
Basic UDI-DI
40495003142KA
EMDN code
V0599 Clinical procedures kits not included in other classes - other
Device class
Class III
System or procedure pack
Procedure pack
EU registration type
System or procedure pack
Medical purpose
A CombiSet is characterized by the customized compilation of defined components used for medical treatments. These are single-use products for surgical procedures.

Manufacturer details

EUDAMED SRN
DE-PR-000019925

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Properties

  • Supplied sterile

Other properties (1)

  • Sterilise before use: No