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DayDrop 5ud x 0.4ml

by i+Med S.Coop. EUDAMED

Active European Union

Ref PV00045Model DayDrop 5ud x 0.4ml

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08437015992150 Basic UDI-DIDate30 Nov 2023RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Expiring

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
DayDrop
Solución oftálmica con ectoína (GOECT) / Ectoine ophthalmic solution (GOECT)
Model / Reference
DayDrop 5ud x 0.4ml, PV00045
Primary DI / UDI-DI
08437015992150
Basic UDI-DI
B-08437015992150, 8437015992OP0045P
EMDN Code
Q02030206 Eye lubricant solutions
Device Class
Class IIa
Class IIb
Market of Registration
Spain

Manufacturer details

EUDAMED SRN
ES-MF-000008633

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Properties

Show properties
  • Sterile
  • CMR Substance
Other properties (11)
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No