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Tonimer Md Hypertonicbaby Spray

by Dermofarm S.A.U. EUDAMED

Active European Union

Ref I48V01560Model TONIMER MD HYPERTONIC BABY SPRAY

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-I48V01560KB Basic UDI-DIDate8 Oct 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Expiring

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.

Specification

EUDAMED

Model / Reference
TONIMER MD HYPERTONIC BABY SPRAY, I48V01560
Primary DI / UDI-DI
D-I48V01560KB
Basic UDI-DI
B-I48V01560KB
EMDN Code
Q030103 Nasal irrigation solutions
Device Class
Class IIa
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
ES-MF-000026081

Other devices from Dermofarm S.A.U.

See all devices from Dermofarm S.A.U. →

Properties

  • Sterile

Other properties (10)

  • 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