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EziDrops® (Eye & Ear Drops Applicators)

by EziDrops Ltd 3 variants

Ref EziDrops® Eye Drop Applicator Wide Head

Active European Union

CE MDR

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number05060692810047FW Basic UDI-DI 05060692810047UDI-DIDate28 Aug 2026RegisteredStatusActive

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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
EziDrops® Eye Drop Applicator Wide Head
Model / Reference
EziDrops® Eye Drop Applicator Wide Head
Primary DI / UDI-DI
05060692810047
Basic UDI-DI
05060692810047FW
EMDN Code
A13 Applicators for drugs and medical devices not present in other classes
Device Class
Class I
EU 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