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Kompletny Zestaw Do Implantacji Portów

by Mediberg S.r.l. Unipersonale 2 variants

Ref 706025AHGNPLB

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, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8030413FTN22-706CN Basic UDI-DI 08030413338294UDI-DIDate2 Sep 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Sistema Assemblato Chirurgia Vascolare Non Sterile
Model / Reference
706025AHGNPLB
Primary DI / UDI-DI
08030413338294
Basic UDI-DI
8030413FTN22-706CN
EMDN Code
V0599 Clinical procedures kits not included in other classes - other
Device Class
Class I
Medical Purpose
I sistemi assemblati sono impiegati in ambito chirurgico e si configurano come un prodotto monouso non sterile. Il loro scopo è fornire supporto nel contesto degli interventi chirurgici al fine di garantire le migliori condizioni e proteggere gli operatori sanitari e il paziente in sala operatoria da contaminazioni incrociate.

Manufacturer details

EUDAMED SRN
IT-PR-000021994

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Properties

Other properties (1)

  • Sterile: No