Skip to content

Optra-Liv

by Legency Remedies Pvt. Ltd. 8 variants

Ref 137

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-137salinesolutionZN Basic UDI-DI D-137salinesolutionZNUDI-DIDate27 May 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  • Withdrawn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

Device Name
Sodium Chloride Eyewash Solution 0.9% w/v 30 ml
Model / Reference
137
Primary DI / UDI-DI
D-137salinesolutionZN
Basic UDI-DI
B-137salinesolutionZN
EMDN Code
Q02030299 Ophthalmology, liquid fluids - other
Device Class
Class IIa
EU market of registration
Denmark

Manufacturer details

EUDAMED SRN
IN-MF-000010030
Authorised representative
Europecert UG (haftungsbeschränkt) DE-AR-000004974

Other devices from Legency Remedies Pvt. Ltd.

See all devices from Legency Remedies Pvt. Ltd. →

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