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Eva Intima Actisperm

by Ioulia and Irene Tseti Pharmaceutical Laboratories S.A. Greece EUDAMED

Ref EVA INTIMA ACTISPERM

EMDN U0899

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-EVAINTMD33024E Basic UDI-DIDate11 Dec 2023RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Expiring (legacy directive)
  • Not covered

European Union — CE/MDD Expiring (legacy directive)

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Model / Reference
EVA INTIMA ACTISPERM
Primary DI / UDI-DI
D-EVAINTMD33024E
Basic UDI-DI
B-EVAINTMD33024E
EMDN Code
U0899 Gynaecological devices - other
Device Class
Class IIa
Market of Registration
Greece

Manufacturer details

EUDAMED SRN
GR-MF-000032958

Other devices from Ioulia and Irene Tseti Pharmaceutical Laboratories S.A.

See all devices from Ioulia and Irene Tseti Pharmaceutical Laboratories S.A. →

Properties & raw data

Show properties, registry sources and raw records
Other properties (11)
  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED edcba6cd-0be7-4f99-ab7f-82b6edaf6b2a 61 fields · synced 22 Oct 2026