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Ago per Implanter Regolabile, sterile

by Medicap S.r.l Italy EUDAMED

Ref AC02 EMDN K01020199

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805715896TF02H9 Basic UDI-DIDate9 Feb 2023RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • CSQ0002220326 Supplemented

    Quality management system EU MDR

    Issued
    30 Sep 2026
    Expires
    22 Dec 2027
    Reason
    Change approved

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Ago per Implanter Regolabile, sterile
Model / Reference
AC02
Primary DI / UDI-DI
08057158965455
Basic UDI-DI
805715896TF02H9
EMDN Code
K01020199 Minimally invasive surgery surgical instrument kits, single-use - other
Device Class
Class IIa
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000007995

Other devices from Medicap S.r.l

See all devices from Medicap 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 08057158965455|805715896TF02H9 61 fields · synced 24 Oct 2026