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Kit 0º 4K/6K Funda Tubo Filtro Ulpa

by Prim, S.A.

Ref KIT-0-UHD-ULPA

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 Number843404825KITLAPAROSFW Basic UDI-DI 08434048511891UDI-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  • Withdrawn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
KIT-0-UHD-ULPA
Primary DI / UDI-DI
08434048511891
Basic UDI-DI
843404825KITLAPAROSFW
EMDN Code
T030203 Optics covers
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