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Unisept Implants Mouthwash

by Ioulia and Irene Tseti Pharmaceutical Laboratories S.A.

Ref UNISEPT IMPLANTS MOUTHWASHModel UNISEPT IMPLANTS MOUTHWASH 250mL, UNISEPT IMPLANTS MOUTHWASH 1.5L

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 26 Oct 2026. What this means

Regulatory status

as of registry sync 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-UNSPTMD2601250KM Basic UDI-DI Date5 Oct 2023RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Model / Reference
UNISEPT IMPLANTS MOUTHWASH 250mL, UNISEPT IMPLANTS MOUTHWASH, UNISEPT IMPLANTS MOUTHWASH 1.5L
Primary DI / UDI-DI
D-UNSPTMD2601250KM, D-UNSPTMD260115002B
Basic UDI-DI
B-UNSPTMD2601250KM, B-UNSPTMD260115002B
EMDN Code
Q0199 Odontology devices - other
Device Class
Class I
EU market of registration
Greece

Manufacturer details

EUDAMED SRN
GR-MF-000032958

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Properties

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