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Senti 2

by Laboratoire d'Odonto-Stomatologie Thermal

Ref PFATP06007Model isotonic

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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-PFATP06007CF Basic UDI-DI D-PFATP06007CFUDI-DIDate16 Jun 2025RegisteredStatusActive

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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device Name
Senti2 agua de mar solucion isotonica Rumano y Arabe 100ml
Model / Reference
isotonic, PFATP06007
Primary DI / UDI-DI
D-PFATP06007CF
Basic UDI-DI
B-PFATP06007CF
EMDN Code
Q030103 Nasal irrigation solutions
Device Class
Class IIa
EU market of registration
Portugal

Manufacturer details

EUDAMED SRN
FR-MF-000011980

Other devices from Laboratoire d'Odonto-Stomatologie Thermal

See all devices from Laboratoire d'Odonto-Stomatologie Thermal →

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