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400-111MR

by MEDI-LINE S.r.l. Italy EUDAMED

Ref 400-111MRModel ACTIVA

EMDN K01020104

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805511288K01020104MF Basic UDI-DIDate2 Dec 2025RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • CSQ0003220524 Supplemented

    Quality management system EU MDR

    Notified body
    ISTITUTO SUPERIORE DI SANITA' 0373
    Issued
    26 Nov 2024
    Expires
    27 Dec 2027
    Reason
    Add device or group

Specification

EUDAMED · synced 24 Oct 2026

Model / Reference
ACTIVA, 400-111MR
Primary DI / UDI-DI
08055112881612
Basic UDI-DI
805511288K01020104MF
EMDN Code
K01020104 Minimally invasive surgery forceps, single-use
Device Class
Class IIb
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000019935

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

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

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
Other properties (12)
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED 08055112881612|805511288K01020104MF 61 fields · synced 24 Oct 2026