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EziDrops® (Eye & Ear Drops Applicators)

by EziDrops Ltd EUDAMED

Active European Union

Ref EziDrops Ear Applicator

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number05060692810054FT Basic UDI-DIDate24 Aug 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

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

Specification

EUDAMED

Model / Reference
EziDrops Ear Applicator
Primary DI / UDI-DI
05060692810054
Basic UDI-DI
05060692810054FT
EMDN Code
A13 Applicators for drugs and medical devices not present in other classes
Device Class
Class I
Market of Registration
Greece

Manufacturer details

EUDAMED SRN
UK-MF-000040365
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

From the manufacturer

Manufacturer's product page: of the EziDrops Eye & Ear Drop Applicators

Other devices from EziDrops Ltd

Properties

  • Administering Medicine

Other properties (12)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No