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Císařský řez

by Paul Hartmann AG 7 variants

Part of a family of 804 devices: see the family page

Ref 2344532Model 3147

Císařský řez (2344532) is a Class III device made by Paul Hartmann AG, registered in EUDAMED on 27 May 2026 (Basic UDI-DI 40495003147KL), active as of 24 Oct 2026.

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

Source EUDAMED, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number40495003147KL Basic UDI-DI 04099467223745UDI-DIDate27 May 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
CombiSet Gynecology and Obstetrics
Model / reference
3147, 2344532
Primary DI / UDI-DI
04099467223745
Basic UDI-DI
40495003147KL
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

Similar devices in this category

Other devices filed under CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER.

Other devices from Paul Hartmann AG

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Properties

  • Supplied sterile
Other properties (1, all answered No)