Skip to content

Xailin® TEARS 0, 1% HA (free sample)

by SUPROBION Sp. z o.o.

Ref 11352_EN_FR_SR_AR_sModel Lubricating eye drops with sodium hyaluronate 0,1% and borate buffer with no preservatives

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05900741962641 Basic UDI-DI 05900741962641UDI-DIDate7 Oct 2026RegisteredStatusActive

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.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Model / Reference
Lubricating eye drops with sodium hyaluronate 0, 1% and borate buffer with no preservatives, 11352_EN_FR_SR_AR_s
Primary DI / UDI-DI
05900741962641
Basic UDI-DI
B-05900741962641
EMDN Code
Q02030301 Ophthalmology, hyaluronic acid and derivatives
Device Class
Class IIa
EU market of registration
Ireland

Manufacturer details

EUDAMED SRN
PL-MF-000018264

Other devices from SUPROBION Sp. z o.o.

See all devices from SUPROBION Sp. z o.o. →

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