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Kit VERESS+4 Trocar C/C+tij

by Prim, S.A.

Ref LAP-209A

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number843404825KITLAPAROSIIBKB Basic UDI-DI 08434048377886UDI-DIDate22 Apr 2025RegisteredStatusActive

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  • Withdrawn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 IIb
Model / Reference
LAP-209A
Primary DI / UDI-DI
08434048377886
Basic UDI-DI
843404825KITLAPAROSIIBKB
EMDN Code
K0201011102 Laparoscopic and thoracoscopic electrosurgery instrument kits, single-use
Device Class
Class IIb
Medical Purpose
Procedure packs that bring together some of the disposable devices needed to carry out laparoscopic surgeries including electrosurgical instrument to retrieve and handle soft tissues into class IIb, with different configurations according to the needs of the services and centres

Manufacturer details

EUDAMED SRN
ES-PR-000004648

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Properties

Other properties (1)

  • Sterile: No