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Liquifilm Tears

by Allergan Sales, LLC 5 variants

Ref 95396FQ

Expiring European Union

CE MDR

Valid until

6 May 2027

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier DEKRA Certification B.V.

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/MDR Number0840228300034F Basic UDI-DI 10840228302404UDI-DIDate4 Aug 2025RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 3829879CE01 Expiring Expires in 185 days

    Quality management system EU MDR

    Certifier
    DEKRA Certification B.V. 0344
    Issued
    6 May 2022
    Expires
    6 May 2027

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Expiring

Specification

EUDAMED

Device Name
Dry Eye Comfort Solutions and Ointments
Model / Reference
95396FQ
Primary DI / UDI-DI
10840228302404
Basic UDI-DI
0840228300034F
Direct Marketing DI
10840228302404
EMDN Code
Q02030206, Q02030299, Q0299
Device Class
Class IIb
EU market of registration
Finland

Manufacturer details

EUDAMED SRN
US-MF-000001517
Authorised representative
Allergan Pharmaceuticals International Limited IE-AR-000000650

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See all devices from Allergan Sales, LLC →

Properties

  • Sterile
  • Administering Medicine

Other properties (11)

  • 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