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Kit Trocar DIL.HASSON+2/11+2/5

by Prim, S.A.

Ref LAP-102

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 Number843404825KITLAPAROSFW Basic UDI-DI 08426680985512UDI-DIDate5 Sep 2022RegisteredStatusActive

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  • Withdrawn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
Agrupaciones Laparoscópicas IIa
Model / Reference
LAP-102
Primary DI / UDI-DI
08426680985512
Basic UDI-DI
843404825KITLAPAROSFW
EMDN Code
K01010102 Hasson trocar, single-use
Device Class
Class IIa
Medical Purpose
Procedure packs for laparoscopic procedures comprising the disposable devices to be used. Different components according to the procedures.

Manufacturer details

EUDAMED SRN
ES-PR-000004648

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Properties

Other properties (1)

  • Sterile: No