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Neovac Set Irrigazione/Aspirazione laparoscopico

by MEDI-LINE S.r.l. 5 variants

Ref 0223Model Neovac

Active European Union

CE MDR

Valid until

27 Dec 2027

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier ISTITUTO SUPERIORE DI SANITA'

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 NumberCSQ0003220524 Date26 Nov 2024IssuedStatusActive expires 27 Dec 2027

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • CSQ0003220524 Active Supplemented

    Quality management system EU MDR

    Issued
    26 Nov 2024
    Expires
    27 Dec 2027
    Reason
    Add device or group

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Neovac Set Irrigazione/Aspirazione laparoscopico
Model / Reference
Neovac, 0223
Primary DI / UDI-DI
08055112881728
Basic UDI-DI
805511288K01020110MA
EMDN Code
K01020110 Minimally invasive surgery cannulas, single-use
Device Class
Class IIa
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000019935

From the manufacturer

Manufacturer's product page: NEOVAC

Other devices from MEDI-LINE S.r.l.

See all devices from MEDI-LINE S.r.l. →

Properties

  • Sterile
  • Administering Medicine

Other properties (11)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No