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Sida-Visc

by SIDAPHARM Private Company

Ref 11030Model SIDA-VISC DYAD

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 linked in EUDAMED

A group certificate may exist

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 Number521301331VISC3E Basic UDI-DI 05213013314889UDI-DIDate21 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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
Sodium Hyaluronate Ophthalmic Solutions Set
Model / Reference
SIDA-VISC DYAD, 11030
Primary DI / UDI-DI
05213013314889
Basic UDI-DI
521301331VISC3E
EMDN Code
Q02030301 Ophthalmology, hyaluronic acid and derivatives
Device Class
Class IIb
Medical Purpose
SIDA-VISC is indicated for use as a space occupying tissue protective fluid and lubricant during various intraocular surgical procedures including intra-/ extracapsular cataract extraction, IOL implants and corneal transplantations. In surgical procedures in the anterior segment of the eye, instillation of the SIDA-VISC serves to maintain a deep anterior chamber during surgery, allowing for efficient manipulation with fewer traumas to the corneal endothelium and other surrounding tissues.

Manufacturer details

EUDAMED SRN
EL-PR-000050928

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Properties

  • Sterile