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Cappetta definitiva Gekon A

by New Ancorvis SRL 4 variants

Ref CKATWMY4, CKCAMY4, CKATPMY4, CKCAMY6, CKATPMY6, CKATModel Cappetta definitiva Gekon A

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8053876-01-015NC Basic UDI-DI Date2 Oct 2023RegisteredStatusActive

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  • Withdrawn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
Cappetta definitiva Gekon A
Model / Reference
Cappetta definitiva Gekon A, CKATWMY4, CKCAMY4, CKATPMY4, CKCAMY6, CKATPMY6, CKAT
Primary DI / UDI-DI
08053876095160, 08053876055997, 08053876055959, 08053876056000, 08053876055966, 08053876048043
Basic UDI-DI
8053876-01-015NC
EMDN Code
Q010299, P0180
Device Class
Class IIa
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000008879

Other devices from New Ancorvis SRL

See all devices from New Ancorvis SRL →

Properties

Other properties (13)

  • Sterile: No
  • 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